Correlation of a recurrent FBN1 mutation (R122C) with an atypical familial marfan syndrome phenotype

Black, Cheryl, Withers, Anne P., Gray, Jonathon, Bridges, Allan B., Craig, Ashley, Baty, David U. and Boxer, Maureen 1998. Correlation of a recurrent FBN1 mutation (R122C) with an atypical familial marfan syndrome phenotype. Human Mutation 11 (S1) , S198-S200. 10.1002/humu.1380110164

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Item Type:	Article
Status:	Published
Schools:	Medicine
Subjects:	R Medicine > R Medicine (General)
Publisher:	Wiley-Blackwell
ISSN:	1059-7794
Last Modified:	19 Mar 2016 23:55
URI:	https://orca.cardiff.ac.uk/id/eprint/72707

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