PROGERIA SYNDROME: FTI'S Approaches For Progeria Syndrome Clinical Trials Case Reports Year wise Events
Dave, Vivek; Paliwal, Dr.Sarvesh; Kr.Vishwakarma, Pushpendra
ISBN 10: 363932210X ISBN 13: 9783639322101
Published by VDM Verlag Dr. Müller, 2010
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Synopsis:
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.
About the Author:
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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Bibliographic Details
Title: PROGERIA SYNDROME: FTI'S Approaches For ...
Publisher: VDM Verlag Dr. Müller
Publication Date: 2010
Binding: Soft cover
Condition: New
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PROGERIA SYNDROME: FTI'S Approaches For Progeria Syndrome Clinical Trials Case Reports Year wise Events
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Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - 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. Seller Inventory # 9783639322101
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Progeria Syndrome
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Progeria Syndrome
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VDM Verlag Dr. Mueller Aktiengesellschaft & Co. KG, 2010
ISBN 10: 363932210X
ISBN 13: 9783639322101
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