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Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome.

ABSTRACT:

SUBMITTER: Zhian S 

PROVIDER: S-EPMC3402694 | biostudies-literature | 2012 Aug

REPOSITORIES: biostudies-literature

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Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome.

Zhian Samaneh S   Belmont John J   Maslen Cheryl L CL  

American journal of medical genetics. Part A 20120627 8

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