Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss

American Journal of Human Genetics

Volumn 78, Issue 1, 2006, Pages 144-152

  Shahin, Hashem ^a,b   Walsh, Tom ^c   Sobe, Tama ^b   Abu Sa'ed, Judeh ^a   Abu Rayan, Amal ^a   Lynch, Eric D ^c   Lee, Ming K ^c   Avraham, Karen B ^b   King, Mary Claire ^c   Kanaan, Moein ^a  

^a Bethlehem University   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

^c UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; PROTEIN SH3;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; GENE; GENE EXPRESSION PROFILING; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC CONSERVATION; HEARING LOSS; HUMAN; MISSENSE MUTATION; MULTIGENE FAMILY; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN LOCALIZATION; SENSORY NERVE CELL; STEREOCILIUM; TRIOBP GENE;

EID: 29244481972     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/499495     Document Type: Article

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