Genetic causes of moderate to severe hearing loss point to modifiers

Clinical Genetics

Volumn 91, Issue 4, 2017, Pages 589-598

  Naz, S ^a   Imtiaz, A ^a,b   Mujtaba, G ^a   Maqsood, A ^a   Bashir, R ^a   Bukhari, I ^a   Khan, M R ^a   Ramzan, M ^a   Fatima, A ^a   Rehman, A U ^b   Iqbal, M ^a   Chaudhry, T ^b   Lund, M ^b   Brewer, C C ^b   Morell, R J ^b   Friedman, T B ^b  

^a UNIVERSITY OF THE PUNJAB   (Pakistan)

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

Author keywords

deafness; DFNB; etiology; hearing loss; modifiers; mutation; Pakistan

Indexed keywords

BSND PROTEIN; CDH23 PROTEIN; CLDN14 PROTEIN; CONNEXIN 26; DFNB32 PROTEIN; DFNB59 PROTEIN; ESPN PROTEIN; GENOMIC DNA; GIPC3 PROTEIN; GPSM2 PROTEIN; GRXCR2 PROTEIN; HGF PROTEIN; MYOSIN VI; MYOSIN VIIA; OTOF PROTEIN; PENDRIN; PROTEIN; PTPRQ PROTEIN; SCATTER FACTOR RECEPTOR; TECTA PROTEIN; TMC1 PROTEIN; TMPRSS3 PROTEIN; TPRN PROTEIN; TRIOBP PROTEIN; UNCLASSIFIED DRUG; USH1C PROTEIN; USH1G PROTEIN;

ARTICLE; AUDITORY THRESHOLD; CONSANGUINEOUS MARRIAGE; DISEASE SEVERITY; FRAMESHIFT MUTATION; GENE FREQUENCY; GENE MAPPING; GENETIC VARIABILITY; HEARING IMPAIRMENT; HOMOZYGOSITY; HUMAN; INDEL MUTATION; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MOLECULAR PATHOLOGY; PRIORITY JOURNAL; SANGER SEQUENCING; WHOLE EXOME SEQUENCING; ADOLESCENT; ADULT; CHILD; EXOME; FEMALE; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; HIGH THROUGHPUT SEQUENCING; MALE; MUTATION; PATHOPHYSIOLOGY; PEDIGREE; PERCEPTION DEAFNESS; PRESCHOOL CHILD; RECESSIVE GENE; SEVERITY OF ILLNESS INDEX; SINGLE NUCLEOTIDE POLYMORPHISM; YOUNG ADULT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; EXOME; FEMALE; GENES, RECESSIVE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HEARING LOSS, SENSORINEURAL; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MALE; MUTATION; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEVERITY OF ILLNESS INDEX; YOUNG ADULT;

EID: 84990852200     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12856     Document Type: Article

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