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Genetic analysis reveals clues to autism's roots

โœ Scribed by Laura Sanders


Book ID
124631661
Publisher
Society for Science & the Public
Year
2011
Tongue
English
Weight
645 KB
Volume
179
Category
Article
ISSN
0036-8423

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## Abstract Schnyder crystalline corneal dystrophy (SCCD) is a rare autosomal dominant disease characterized by progressive corneal opacification resulting from abnormal deposition of cholesterol and phospholipids. Recently, six different mutations on the __UBIAD1__ gene on chromosome 1p36 were fou