Studies on cultured fibroblasts from patients with defects of biotin-dependent carboxylation

Author:

Bartlett K.,Ng H.,Dale G.,Green A.,Leonard J. V.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The Further Adventures of Newborn Screening for Biotinidase Deficiency: Where It Is at and What We Still Need to Know;International Journal of Neonatal Screening;2016-10-28

2. Multiple carboxylase deficiency/holocarboxylase synthetase deficiency;Atlas of Inherited Metabolic Diseases 3E;2011-12-30

3. Problems in the Congenital Lactic Acidoses;Ciba Foundation Symposium 87 - Metabolic Acidosis;2008-05-30

4. Dermatologic Signs of Biotin Deficiency Leading to the Diagnosis of Multiple Carboxylase Deficiency;Pediatric Dermatology;2004-05

5. Holocarboxylase Synthetase;Wiley Encyclopedia of Molecular Medicine;2002-01-15

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