BIOTIN-RESPONSIVE β-METHYLCROTONYLGLYCINURIA
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G. Draffan | D. Gompertz | J. Watts | D. Hull
[1] E. Delvin,et al. Thiamine-responsive maple-syrup-urine disease. , 1971, Lancet.
[2] K. Isselbacher,et al. EXPERIMENTAL β-HYDROXYISOVALERIC ACIDURIA INDUCED BY BIOTIN DEFICIENCY , 1970 .
[3] E. Jellum,et al. Beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria: a new inborn error of metabolism. , 1970, Lancet.
[4] D. Gompertz,et al. Biotin-responsive propionicacidaemia. , 1970, Lancet.
[5] H. Harris. Genetical theory and the "inborn errors of metabolism". , 1970, British medical journal.
[6] L. Rosenberg,et al. Methylmalonic Aciduria: Metabolic Block Localization and Vitamin B12 Dependency , 1968, Science.
[7] K. Isselbacher,et al. Isovaleric acidemia: a new genetic defect of leucine metabolism. , 1966, Proceedings of the National Academy of Sciences of the United States of America.