CORRELATION OF A RECURRENT FBN1 MUTATION (R122C) WITH AN ATYPICAL FAMILIAL MARFAN-SYNDROME PHENOTYPE

Authors
BLACK C WITHERS AP GRAY JR BRIDGES AB CRAIG A BATY DU BOXER M
Citation
C. Black et al., CORRELATION OF A RECURRENT FBN1 MUTATION (R122C) WITH AN ATYPICAL FAMILIAL MARFAN-SYNDROME PHENOTYPE, Human mutation, 1998, pp. 198-200
Citations number
12
Categorie Soggetti
Genetics & Heredity
Journal title
Human mutation → ACNP
ISSN journal
10597794
Year of publication
1998
Supplement
1
Pages
198 - 200
Database
ISI
SICI code
1059-7794(1998):<198:COARFM>2.0.ZU;2-K