Molecular effects of homocysteine on cbEGF domain structure: insights into the pathogenesis of homocystinuria.

Homocystinuria is an inborn error of methionine metabolism that results in raised serum levels of the highly reactive thiol-containing amino acid homocysteine. Homocystinurics often exhibit phenotypic abnormalities that are similar to those found in Marfan syndrome (MFS), a heritable connective tiss...

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Bibliographic Details
Main Authors: Hutchinson, S, Aplin, RT, Webb, H, Kettle, S, Timmermans, J, Boers, G, Handford, P
Format: Journal article
Language:English
Published: 2005