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Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome
Author(s) -
Zhian Samaneh,
Belmont John,
Maslen Cheryl L.
Publication year - 2012
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.35457
Subject(s) - missense mutation , medicine , medical genetics , gerontology , genetics , biology , mutation , gene