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Functionally Null Mutations in Patients with the cblG-Variant Form of Methionine Synthase Deficiency

✍ Scribed by A. Wilson; D. Leclerc; F. Saberi; E. Campeau; H.Y. Hwang; B. Shane; J.A. Phillips III; D.S. Rosenblatt; R.A. Gravel

Book ID: 117852514
Publisher: American Society of Human Genetics
Year: 1998
Tongue: English
Weight: 193 KB
Volume: 63
Category: Article
ISSN: 0002-9297
DOI: 10.1086/301976

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