Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29

Cell

Volumn 104, Issue 1, 2001, Pages 165-172

  Wilcox, Edward R ^a   Burton, Quianna L ^a   Naz, Sadaf ^b   Riazuddin, Saima ^a,b   Smith, Tenesha N ^a   Ploplis, Barbara ^a   Belyantseva, Inna ^a   Ben Yosef, Tamar ^a   Liburd, Nikki A ^a   Morell, Robert J ^a   Kachar, Bechara ^a   Wu, Doris K ^a   Griffith, Andrew J ^a   Riazuddin, Sheikh ^b   Friedman, Thomas B ^a  

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

^b UNIVERSITY OF THE PUNJAB   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

CLAUDIN; CLAUDIN 14; COMPLEMENTARY DNA; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CLOSTRIDIUM PERFRINGENS; COCHLEA DUCT; CORTI ORGAN; ENDOLYMPH; GENE EXPRESSION; GENE MUTATION; HEARING IMPAIRMENT; IMMUNOFLUORESCENCE; IN SITU HYBRIDIZATION; MISSENSE MUTATION; MULTIGENE FAMILY; NEUROEPITHELIUM; PRIORITY JOURNAL; PROTEIN INTERACTION; TIGHT JUNCTION;

CLOSTRIDIUM PERFRINGENS;

EID: 17744380785     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(01)00200-8     Document Type: Article

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