High frequency (71%) of cystathionine β-synthase mutation G307S in Irish homocystinuria patients-Reference-Cited by-同舟云学术

High frequency (71%) of cystathionine β-synthase mutation G307S in Irish homocystinuria patients

Published:1995 Issue:2 Volume:6 Page:177-180
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Gallagher Paula M.,Ward Pat,Tan Soon,Naughten Eileen,Kraus Jan P.,Sellar Grant C.,McConnell David J.,Graham Ian,Whitehead Alexander S.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. (1971) The response of patients with cystathionine synthase deficiency to pyridoxine. In (eds): Inherited Disorders of Sulphur Metab olism. London:Churchill Livingstone, p 264.

2. Hyperhomocysteinemia: An Independent Risk Factor for Vascular Disease

3. (1991) International Congress of Human Genetics, Washington 1991, p 2298 (abst).

4. Homocysteine-induced modulation of tissue plasminogen activator binding to its endothelial cell membrane receptor.

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