miRNA mutations are not a common cause of deafness

American Journal of Medical Genetics, Part A

Volumn 152, Issue 3, 2010, Pages 646-652

  Hildebrand, Michael S ^a   Witmer, P Dane ^b   Xu, Shunbin ^c   Newton, Stephen S ^a   Kahrizi, Kimia ^d   Najmabadi, Hossein ^d   Valle, David ^b   Smith, Richard J H ^a,e  

^a UNIVERSITY OF IOWA   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c RUSH UNIVERSITY MEDICAL CENTER   (United States)

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

^e UNIVERSITY OF IOWA   (United States)

Author keywords

ADNSHL; ARNSHL; ERM protein family; miRNA; Radixin

Indexed keywords

MICRORNA; MICRORNA 182; MICRORNA 183; MICRORNA 96; RADIXIN; UNCLASSIFIED DRUG;

3' UNTRANSLATED REGION; ARTICLE; AUTOSOMAL DOMINANT NON SYNDROMIC DEAFNESS; AUTOSOMAL RECESSIVE NON SYNDROMIC HEARING LOSS; BINDING SITE; CONTROLLED STUDY; GENE CLUSTER; GENE CONTROL; GENE EXPRESSION; GENE MUTATION; GENE TARGETING; HUMAN; INNER EAR; MAJOR CLINICAL STUDY; NEUROEPITHELIUM; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RNA SEQUENCE;

3' UNTRANSLATED REGIONS; ANIMALS; BASE SEQUENCE; BINDING SITES; CYTOSKELETAL PROTEINS; DEAFNESS; DNA PRIMERS; FEMALE; GENES, DOMINANT; GENES, RECESSIVE; HOMOZYGOTE; HUMANS; MALE; MEMBRANE PROTEINS; MICE; MICRORNAS; MULTIGENE FAMILY; MUTATION; PEDIGREE; SEQUENCE HOMOLOGY, NUCLEIC ACID;

MUS;

EID: 77649197124     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33299     Document Type: Article

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