Sclerosteosis-1: Clinical and Molecular Studies in an Egyptian Family - Fayez, Alaaeldin;Aglan, Mona;El Ruby, Mona
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We wrote this book for everyone looking for background genetics information about bone growth disorders especially sclerosteosis. Sclerosteosis-1 is an autosomal recessive disorder characterized by bone overgrowth due to aberrant Sclerostin protein, the product of the SOST gene. This book describes the clinical and molecular studies for the first reported affected Egyptian family with sclerosteosis-1 including novel variant and a new expanding clinical feature. I believe that the book will be a valuable resource for researchers and students looking for study of human SOST-related sclerosing bone dysplasia disorders.…mehr

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Produktbeschreibung
We wrote this book for everyone looking for background genetics information about bone growth disorders especially sclerosteosis. Sclerosteosis-1 is an autosomal recessive disorder characterized by bone overgrowth due to aberrant Sclerostin protein, the product of the SOST gene. This book describes the clinical and molecular studies for the first reported affected Egyptian family with sclerosteosis-1 including novel variant and a new expanding clinical feature. I believe that the book will be a valuable resource for researchers and students looking for study of human SOST-related sclerosing bone dysplasia disorders.
Autorenporträt
Alaaeldin Gamal Fayez, Doctor:Profesor Asociado de Genética Molecular Médica,División de Genética Humana e Investigación Genómica - Centro de Excelencia de Genética Humana - Centro Nacional de Investigación, El-Bohous Street El-Dokki Cairo, 12622, Egipto.