Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patients
- 12 December 1995
- journal article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1272 (3) , 168-174
- https://doi.org/10.1016/0925-4439(95)00082-8
Abstract
No abstract availableKeywords
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