Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models

Brain Research

Volumn 1277, Issue , 2009, Pages 52-69

  Hoang Dinh, Emilie ^a   Ahmad, Shoeb ^a   Chang, Qing ^a   Tang, Wenxue ^a   Stong, Benjamin ^a   Lin, Xi ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Connexin mutation; Deafness mechanism; Gap junction function; Inherited deafness; Review

Indexed keywords

CONNEXIN 26; CONNEXIN 30; CONNEXIN 31; CONNEXIN 32; CONNEXIN 43; CONNEXIN 45; GAP JUNCTION PROTEIN; MEMBRANE PROTEIN; PANNEXIN; UNCLASSIFIED DRUG;

ANIMAL MODEL; CELL DEATH; CELL MEMBRANE; COCHLEA; DISEASE CLASSIFICATION; GENE MUTATION; HEARING IMPAIRMENT; IN VITRO STUDY; MOUSE; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN STRUCTURE; REVIEW;

ANIMALS; COCHLEA; CONNEXINS; DEAFNESS; DISEASE MODELS, ANIMAL; GAP JUNCTIONS; HUMANS; MICE; MODELS, BIOLOGICAL; MUTATION; POTASSIUM;

MUS;

EID: 67349248636     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2009.02.008     Document Type: Review

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