Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

Nature Genetics

Volumn 27, Issue 1, 2001, Pages 103-107

  Palma, Federica Di ^a   Holme, Ralph H ^b   Bryda, Elizabeth C ^c   Belyantseva, Inna A ^a   Pellegrino, Richard ^a   Kachar, Bechara ^a   Steel, Karen P ^b   Noben Trauth, Konrad ^a  

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

^b MRC INSTITUTE OF HEARING RESEARCH   (United Kingdom)

^c MARSHALL UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; COMPLEMENTARY DNA;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHROMOSOME 10; GENE MUTATION; HEARING IMPAIRMENT; INNER EAR; MOUSE; NEUROEPITHELIUM; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; STEREOCILIUM; USHER SYNDROME;

AMINO ACID SEQUENCE; ANIMALS; AUDITORY PERCEPTION; BASE SEQUENCE; CADHERINS; CLONING, MOLECULAR; COCHLEA; DISEASE MODELS, ANIMAL; DNA MUTATIONAL ANALYSIS; HAIR CELLS, INNER; HEARING; HEARING LOSS, SENSORINEURAL; HEARING TESTS; IN SITU HYBRIDIZATION; MICE; MICE, INBRED STRAINS; MICE, MUTANT STRAINS; MICROSCOPY, ELECTRON, SCANNING; MOLECULAR SEQUENCE DATA; MUTATION; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; SYNDROME;

ANIMALIA; RODENTIA;

EID: 0035168151     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/83660     Document Type: Article

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