Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 8, 2012, Pages 1857-1864

  Fattahi, Zohreh ^a   Shearer, A Eliot ^b   Babanejad, Mojgan ^a   Bazazzadegan, Niloofar ^a   Almadani, Seyed Navid ^c   Nikzat, Nooshin ^a   Jalalvand, Khadijeh ^a   Arzhangi, Sanaz ^a   Esteghamat, Fatemehsadat ^a   Abtahi, Rezvan ^d   Azadeh, Batool ^e   Smith, Richard J H ^b   Kahrizi, Kimia ^a   Najmabadi, Hossein ^a  

^a UNIVERSITY OF SOCIAL WELFARE AND REHABILITATION SCIENCES   (Iran)

^b UNIVERSITY OF IOWA   (United States)

^c ROYAN INSTITUTE FOR REPRODUCTIVE BIOMEDICINE   (Iran)

^d Saveh Welfare Organization   (Iran)

^e Isfahan Welfare Organization   (Iran)

Author keywords

Autosomal recessive nonsyndromic hearing loss; DFNB3; Iran; Myo15A

Indexed keywords

MYOSIN; MYOSIN XV PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; ASIAN; AUTOSOMAL RECESSIVE DISORDER; CHILD; COHORT ANALYSIS; CONTROLLED STUDY; FAMILY STUDY; GENE; GENE DELETION; GENE FREQUENCY; GENE LOCUS; GENETIC LINKAGE; GJB2 GENE; HEARING IMPAIRMENT; HUMAN; IRANIAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTATIONAL ANALYSIS; MYO15A GENE; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; POPULATION GENETICS; POPULATION RESEARCH; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DEAFNESS; FEMALE; GENES, RECESSIVE; HUMANS; IRAN; MALE; MUTATION; MYOSINS; PEDIGREE;

MUS;

EID: 84864151320     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34411     Document Type: Article

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