Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23)

Gene

Volumn 281, Issue 1-2, 2001, Pages 31-41

  Di Palma, Federica ^a   Pellegrino, Richard ^a   Noben Trauth, Konrad ^a  

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

Author keywords

Age related hearing loss; Deafness; Usher syndrome type 1D; Waltzer

Indexed keywords

MUTANT PROTEIN; NERVE CELL ADHESION MOLECULE;

ALLELE; AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME 10; CORTI ORGAN; EXON; GENE EXPRESSION; GENE FUNCTION; GENE LOCUS; GENE MUTATION; GENE STRUCTURE; GENETIC TRANSCRIPTION; HEARING IMPAIRMENT; HEARING LOSS; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN SECONDARY STRUCTURE; SEQUENCE ANALYSIS;

3' UNTRANSLATED REGIONS; 5' UNTRANSLATED REGIONS; ALLELES; ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BINDING SITES; CADHERINS; EXONS; GENES; INTRONS; MICE; MICE, INBRED BALB C; MICE, INBRED C57BL; MICE, INBRED CBA; MICE, INBRED DBA; MICE, INBRED NOD; MICE, INBRED STRAINS; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN ISOFORMS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0035960929     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(01)00761-2     Document Type: Article

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