Methionine Adenosyltransferase I/III Deficiency: Novel Mutationsand Clinical Variations-Reference-Cited by-同舟云学术

Methionine Adenosyltransferase I/III Deficiency: Novel Mutationsand Clinical Variations

Published:2000-02 Issue:2 Volume:66 Page:347-355
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Chamberlin Margaret E.,Ubagai Tsuneyuki,Mudd S. Harvey,Thomas Janet,Pao Vivian Y.,Nguyen Thien K.,Levy Harvey L.,Greene Carol,Freehauf Cynthia,Chou Janice Yang

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference26 articles.

1. Characterization of a full-length cDNA encoding human liver S-adenosylmethionine synthetase: tissue-specific gene expression and mRNA levels in hepatopathies;Alvarez;Biochem J,1993

2. Persistent hypermethioninaemia with dominant inheritance;Blom;J Inherit Metab Dis,1992

3. S-adenosylmethionine: a new intermediate formed enzymatically from L-methionine and adenosinetriphosphate;Cantoni;J Biol Chem,1953

4. Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene;Chamberlin;Am J Hum Genet,1997

5. Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency;Chamberlin;J Clin Invest,1996

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