Auditory function and the M34T allele of Connexin 26 [5]

Archives of Otolaryngology - Head and Neck Surgery

Volumn 128, Issue 1, 2002, Pages 94-

  Griffith, Andrew J ^a   Friedman, Thomas B ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GENE PRODUCT; PROTEIN M34T; UNCLASSIFIED DRUG;

ALLELISM; CHILD; CHILDHOOD DISEASE; CORRELATION ANALYSIS; DIAGNOSTIC VALUE; GENE DELETION; GENE MUTATION; GENOTYPE; HEARING; HETEROZYGOSITY; HUMAN; LETTER; MEDICAL LITERATURE; PERCEPTION DEAFNESS;

ALLELES; CHILD; CONNEXINS; DEAFNESS; HUMANS;

EID: 0036142616     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (4)

1. Connexin 26 gene mutations in congenitally deaf children: Pitfalls for genetic counseling
2. Autosomal recessive nonsyndromic neurosensory deafness at DFNBI not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT
3. Genetic analysis of the connexin-26 M34T variant
4. Mutation screening for deafness: More than simply another diagnostic test