A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1

Clinical Genetics

Volumn 73, Issue 4, 2008, Pages 367-372

  Peters, L M ^a   Fridell, R A ^b   Boger, E T ^a   San Agustin, T B ^c   Madeo, A C ^a   Griffith, A J ^a   Friedman, T B ^a   Morell, R J ^a  

^a NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

^b BRISTOL MYERS SQUIBB   (United States)

^c Office of Special Education and Rehabilitative Services   (United States)

Author keywords

DFNA27; Genetic linkage; Inner ear; Non syndromic hearing loss

Indexed keywords

GAP JUNCTION PROTEIN; PROTEIN DFNA27; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 4Q; CHROMOSOME ANALYSIS; CHROMOSOME DISORDER; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENE LOCUS; GENE SEQUENCE; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETIC SCREENING; GENOME ANALYSIS; HUMAN; MAJOR CLINICAL STUDY; MALE; PATIENT ASSESSMENT; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS; PREDICTION; PRIORITY JOURNAL;

ADULT; AGED; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; GENES, DOMINANT; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; PEDIGREE;

EID: 40749100281     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2008.00966.x     Document Type: Article

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