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Glutaric aciduria; A “new” disorder of amino acid metabolism

✍ Scribed by Stephen I. Goodman; Sanford P. Markey; Paul G. Moe; Barbara S. Miles; Cecilia C. Teng


Book ID
115766449
Publisher
Elsevier Science
Year
1975
Tongue
English
Weight
561 KB
Volume
12
Category
Article
ISSN
0006-2944

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## Abstract Glutaric aciduria type 1 (GA1) is an autosomal recessive neurometabolic disorder due to glutaryl CoA dehydrogenase deficiency. Comprehensive descriptions of GA1‐associated movement disorders are rare. In order to refine the description of the motor phenotype, we prospectively studied 16