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Pyruvate dehydrogenase complex deficiency due to a point mutation (P188L) within the thiamine pyrophosphate binding
S G Hemalatha1, D S Kerr, I D Wexler
1Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Human Molecular Genetics
|February 1, 1995
Abstract
No abstract available in PubMed .
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