Hyperhomocysteinemia Due to Methionine Synthase Deficiency, cblG: Structure of the MTR Gene, Genotype Diversity, and Recognition of a Common Mutation, P1173L-Reference-Cited by-同舟云学术

Hyperhomocysteinemia Due to Methionine Synthase Deficiency, cblG: Structure of the MTR Gene, Genotype Diversity, and Recognition of a Common Mutation, P1173L

Published:2002-07 Issue:1 Volume:71 Page:143-153
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Watkins David,Ru Ming,Hwang Hye-Yeon,Kim Caroline D.,Murray Angus,Philip Noah S.,Kim William,Legakis Helen,Wai Timothy,Hilton John F.,Ge Bing,Doré Carole,Hosack Angela,Wilson Aaron,Gravel Roy A.,Shane Barry,Hudson Thomas J.,Rosenblatt David S.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference34 articles.

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5. Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects;Christensen;Am J Med Genet,1999

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