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

Samaneh Zhian, John Belmont, Cheryl Maslen

    Research output: Contribution to journalArticle

    10 Citations (Scopus)
    Original languageEnglish (US)
    Pages (from-to)2047-2049
    Number of pages3
    JournalAmerican Journal of Medical Genetics, Part A
    Volume158 A
    Issue number8
    DOIs
    StatePublished - Aug 2012

    Fingerprint

    Heart Septal Defects
    Heterotaxy Syndrome
    Extracellular Matrix Proteins
    Ventricular Heart Septal Defects
    Cell Adhesion Molecules
    Missense Mutation
    Mutation
    Atrioventricular Septal Defect

    ASJC Scopus subject areas

    • Genetics(clinical)
    • Genetics

    Cite this

    Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome. / Zhian, Samaneh; Belmont, John; Maslen, Cheryl.

    In: American Journal of Medical Genetics, Part A, Vol. 158 A, No. 8, 08.2012, p. 2047-2049.

    Research output: Contribution to journalArticle

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