Functionally Null Mutations in Patients with the cblG-Variant Form of Methionine Synthase Deficiency
- 1 August 1998
- journal article
- case report
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 63 (2), 409-414
- https://doi.org/10.1086/301976
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
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