Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiency-Reference-Cited by-同舟云学术

Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiency

Published:2010-02-11 Issue:5 Volume:78 Page:441-448
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Urreizti R,Moya-García AA,Pino-Ángeles A,Cozar M,Langkilde A,Fanhoe U,Esteves C,Arribas J,Vilaseca MA,Pérez-Dueñas B,Pineda M,González V,Artuch R,Baldellou A,Vilarinho L,Fowler B,Ribes A,Sánchez-Jiménez F,Grinberg D,Balcells S

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01391.x/fullpdf

Reference44 articles.

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3. Homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency revealed by stroke in adult siblings;Visy;Neurology,1991

4. Methylenetetrahydrofolate reductase;Rosenblatt;Clin Invest Med,2001

5. Psychosis, paraplegia and coma revealing methylenetetrahydrofolate reductase deficiency in a 56-year-old woman;Michot;J Neurol Neurosurg Psychiatry,2008

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