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Jacinta L. Chuang

University of Texas at Dallas

8

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177

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Branched-Chain Amino Acids : Metabolism , Physiological Function , and Application Lessons from Genetic Disorders of Branched-Chain Amino Acid Metabolism 1 – 3

2005
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Rare Etiology of Autosomal Recessive Disease in a Child with Noncarrier Parents

2000 American Journal of Human Genetics
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Molecular and biochemical basis of intermediate maple syrup urine disease. Occurrence of homozygous G245R and F364C mutations at the E1 alpha locus of Hispanic-Mexican patients.

1995 Journal of Clinical Investigation
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Molecular basis of maple syrup urine disease and stable correction by retroviral gene transfer : Alpha-keto acid dehydrogenase complexes : nutrient control, gene regulation and genetic defects

1995 Journal of Nutrition
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