PROGERIA SYNDROME: FTI'S Approaches For Progeria Syndrome Clinical Trials Case Reports Year wise Events

 
9783639322101: PROGERIA SYNDROME: FTI'S Approaches For Progeria Syndrome Clinical Trials Case Reports Year wise Events

Progeria (also known as "Hutchinson?Gilford progeria syndrome" and "Hutchinson?Gilford syndrome") is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. The disease has a very low incidence and occurs in one per eight million live births.Those born with progeria typically live about thirteen years, although many have been known to live into their late teens and early twenties and rare individuals may even reach their forties. It is a genetic condition that occurs as a new mutation and is not usually inherited, although there is a uniquely inheritable form. This is in contrast to another rare but similar premature aging syndrome, dyskeratosis congenita (DKC), which is inheritable and will often be expressed multiple times in a family line.

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Vivek Dave have done M.Pharm in Pharmaceutics from manipal college of pharmaceutical sciences,India. He is perusing Ph.D. from Banasthali University, Jaipur, India. His research interest in delivery of various drugs through transdermal, nanoparticle&ocular route.

Vivek Dave have done M.Pharm in Pharmaceutics from manipal college of pharmaceutical sciences,India. He is perusing Ph.D. from Banasthali University, Jaipur, India. His research interest in delivery of various drugs through transdermal, nanoparticle&ocular route.

Vivek Dave have done M.Pharm in Pharmaceutics from manipal college of pharmaceutical sciences,India. He is perusing Ph.D. from Banasthali University, Jaipur, India. His research interest in delivery of various drugs through transdermal, nanoparticle&ocular route.

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Book Description Book Condition: New. Publisher/Verlag: VDM Verlag Dr. Müller | FTI'S Approaches For Progeria Syndrome Clinical Trials Case Reports Year wise Events | Progeria (also known as "Hutchinson Gilford progeria syndrome" and "Hutchinson Gilford syndrome") is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. The disease has a very low incidence and occurs in one per eight million live births.Those born with progeria typically live about thirteen years, although many have been known to live into their late teens and early twenties and rare individuals may even reach their forties. It is a genetic condition that occurs as a new mutation and is not usually inherited, although there is a uniquely inheritable form. This is in contrast to another rare but similar premature aging syndrome, dyskeratosis congenita (DKC), which is inheritable and will often be expressed multiple times in a family line. | Format: Paperback | Language/Sprache: english | 227 gr | 220x150x9 mm | 172 pp. Bookseller Inventory # K9783639322101

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Book Description VDM Verlag Dez 2010, 2010. Taschenbuch. Book Condition: Neu. Neuware - Progeria (also known as 'Hutchinson Gilford progeria syndrome' and 'Hutchinson Gilford syndrome') is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. The disease has a very low incidence and occurs in one per eight million live births.Those born with progeria typically live about thirteen years, although many have been known to live into their late teens and early twenties and rare individuals may even reach their forties. It is a genetic condition that occurs as a new mutation and is not usually inherited, although there is a uniquely inheritable form. This is in contrast to another rare but similar premature aging syndrome, dyskeratosis congenita (DKC), which is inheritable and will often be expressed multiple times in a family line. 172 pp. Englisch. Bookseller Inventory # 9783639322101

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Book Description VDM Verlag Dez 2010, 2010. Taschenbuch. Book Condition: Neu. Neuware - Progeria (also known as 'Hutchinson Gilford progeria syndrome' and 'Hutchinson Gilford syndrome') is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. The disease has a very low incidence and occurs in one per eight million live births.Those born with progeria typically live about thirteen years, although many have been known to live into their late teens and early twenties and rare individuals may even reach their forties. It is a genetic condition that occurs as a new mutation and is not usually inherited, although there is a uniquely inheritable form. This is in contrast to another rare but similar premature aging syndrome, dyskeratosis congenita (DKC), which is inheritable and will often be expressed multiple times in a family line. 172 pp. Englisch. Bookseller Inventory # 9783639322101

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Book Description VDM Verlag Dez 2010, 2010. Taschenbuch. Book Condition: Neu. This item is printed on demand - Print on Demand Neuware - Progeria (also known as 'Hutchinson Gilford progeria syndrome' and 'Hutchinson Gilford syndrome') is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. The disease has a very low incidence and occurs in one per eight million live births.Those born with progeria typically live about thirteen years, although many have been known to live into their late teens and early twenties and rare individuals may even reach their forties. It is a genetic condition that occurs as a new mutation and is not usually inherited, although there is a uniquely inheritable form. This is in contrast to another rare but similar premature aging syndrome, dyskeratosis congenita (DKC), which is inheritable and will often be expressed multiple times in a family line. 172 pp. Englisch. Bookseller Inventory # 9783639322101

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