Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

American Journal of Human Genetics

Volumn 74, Issue 4, 2004, Pages 770-776

  Donaudy, Francesca ^a   Snoeckx, Rik ^b   Pfister, Markus ^d   Zenner, Hans Peter ^d   Blin, Nikolaus ^e   Di Stazio, Mariateresa ^a   Ferrara, Antonella ^a   Lanzara, Carmen ^a   Ficarella, Romina ^a   Declau, Frank ^c   Pusch, Carsten M ^e   Nürnberg, Peter ^f   Melchionda, Salvatore ^g   Zelante, Leopoldo ^g   Ballana, Ester ^h   Estivill, Xavier ^h   Van Camp, Guy ^b   Gasparini, Paolo ^a   Savoia, Anna ^a  

^a SECOND UNIVERSITY OF NAPLES   (Italy)

^b UNIVERSITY OF ANTWERP   (Belgium)

^c ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^d UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

^e UNIVERSITY OF TÜBINGEN   (Germany)

^f HUMBOLDT UNIVERSITY   (Germany)

^g CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^h CENTRE FOR GENOMIC REGULATION CRG   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ION CHANNEL; MYOSIN HEAVY CHAIN;

ALLELE; ARTICLE; AUDITORY SYSTEM; AUTOSOMAL DOMINANT DISORDER; BELGIUM; CELL ORGANELLE; CHANNEL GATING; COCHLEA; CONTROLLED STUDY; CYTOSKELETON; GENE EXPRESSION; GENE MUTATION; GENE TRANSLOCATION; GENETIC SCREENING; GERMANY; HEARING DISORDER; HUMAN; ITALY; MISSENSE MUTATION; MYH14 GENE; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL; PROCESS MODEL; PROTEIN LOCALIZATION; SPAIN; SYNDROME DELINEATION;

EID: 12144286156     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/383285     Document Type: Article

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