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

Author:

A. Wilson,D. Leclerc,F. Saberi,E. Campeau,H.Y. Hwang,B. Shane,J.A. Phillips,D.S. Rosenblatt,R.A. Gravel

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

August 1998

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