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

Samaneh Zhian, John Belmont, Cheryl L. Maslen

    Research output: Contribution to journalLetterpeer-review

    14 Scopus citations

    Fingerprint

    Dive into the research topics of 'Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome'. Together they form a unique fingerprint.