3p- syndrome defines a hearing loss locus in 3p25.3

Hearing Research

Volumn 224, Issue 1-2, 2007, Pages 51-60

  McCullough, Brendan J ^a   Adams, Joe C ^b   Shilling, Dustin J ^a   Feeney, M Patrick ^a   Sie, Kathleen C Y ^a,c   Tempel, Bruce L ^a  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^b MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^c SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

Author keywords

3p syndrome; ATP2B2; Deafwaddler; Hearing loss; PMCA2

Indexed keywords

ARTICLE; AUDITORY SYSTEM; CELL MEMBRANE; CHILD; CHROMOSOME 3P; CHROMOSOME 3P DELETION SYNDROME; CLINICAL FEATURE; COCHLEA; DISEASE SEVERITY; FEMALE; GENE DELETION; GENE FUNCTION; GENE LOCUS; GENE MAPPING; HAIR CELL; HEARING LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; STEREOCILIUM;

ANIMALS; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; COCHLEA; DISEASE MODELS, ANIMAL; DNA PRIMERS; FEMALE; HEARING LOSS, BILATERAL; HEARING LOSS, SENSORINEURAL; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MICE; MUTATION; PLASMA MEMBRANE CALCIUM-TRANSPORTING ATPASES; SPECIES SPECIFICITY; SYNDROME;

EID: 33846391965     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.heares.2006.11.006     Document Type: Article

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