Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.

Human genetics

Volumn 118, Issue 1, 2005, Pages 29-34

  Makishima, Tomoko ^a   Rodriguez, Clara I ^a   Robertson, Nahid G ^a   Morton, Cynthia C ^a   Stewart, Colin L ^a   Griffith, Andrew J ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

COCH PROTEIN, HUMAN; COCH PROTEIN, MOUSE; PRIMER DNA; PROTEIN;

ANIMAL; ARTICLE; BRAIN STEM; GENETICS; HEARING LOSS; MOUSE; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ANIMALS; BASE SEQUENCE; BRAIN STEM; DNA PRIMERS; HEARING LOSS; MICE; PROTEINS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 33645131227     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-005-0001-4     Document Type: Article

References (0)