Pyruvate dehydrogenase deficiency.

Author:

Brown G K,Otero L J,LeGris M,Brown R M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference24 articles.

1. Isolated and combined deficiencies of the a-keto acid dehydrogenase complexes;Robinson, B.H.; Chun, K.; Mackay, N.; Otulakowski, G.; PetrovaBenedict, R.; Willard, H.;Ann N Y Acad Sci,1989

2. Genetic defects in human pyruvate dehydrogenase;Ho, L.; Wexler, I.D.; Kerr, D.S.; Patel, M.S.;Ann N YAcad Sci,1989

3. The clinical and biochemical spectrum of human pyruvate dehydrogenase deficiency;Brown, G.K.; Brown, R.M.; Scholem, R.D.; Kirby, D.M.; Dahl, H.H.M.;Ann N Y Acad Sci,1989

4. Molecular biology and biochemistry of pyruvate dehydrogenase complexes;Patel, M.S.; Roche, T.E.;FASEB J,1990

5. Variable clinical presentation in patients with defective El component of pyruvate dehydrogenase complex;Robinson, B.H.; MacMillan, H.; Petrova-Benedict, R.; Sherwood, W.G.;J Pediatr,1987

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