Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders
Publication date:
2020
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Citación:
Human Mutation, 41(9), p. 1615-1628 (2020); doi:10.1002/humu.24067
Descripción física:
p. 1615-1628
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DOI:
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Financial assistance was received in support of the study by grants from the German Federal Ministry of Education and Research (BMBF) (GeNeRARe, FKZ: 01GM1519D) to M. Z. and from the Institute of Health Carlos III: Convenio ISCIII‐ASEREMAC, and Fundación 1000 sobre Defectos Congénitos, of Spain to E. B.‐S. and I. R. G.
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