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

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 8, 2012, Pages 2047-2049

  Zhian, Samaneh ^a   Belmont, John ^b   Maslen, Cheryl L ^c  

^a PORTLAND STATE UNIVERSITY   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL SURFACE PROTEIN;

ATRIOVENTRICULAR SEPTAL DEFECT; CRELD1 GENE; DISEASE ASSOCIATION; DNA SEQUENCE; GENE; GENETIC ASSOCIATION; GENETIC DISORDER; HETEROTAXY SYNDROME; HUMAN; LETTER; MISSENSE MUTATION; PATHOGENESIS; PREVALENCE; PRIORITY JOURNAL; PROTEIN STRUCTURE;

CELL ADHESION MOLECULES; EXTRACELLULAR MATRIX PROTEINS; HEART SEPTAL DEFECTS, VENTRICULAR; HETEROTAXY SYNDROME; HUMANS; MUTATION; MUTATION, MISSENSE; SYNDROME;

EID: 84864148822     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35457     Document Type: Letter

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