A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus

Human Molecular Genetics

Volumn 4, Issue 12, 1995, Pages 2391-2394

  Jain, Pawan K ^f   Fukushima, Kunihiro ^a   Deshmukh, Dilip ^b   Ramesh, Arabandi ^c   Thomas, Elizabeth ^d   Lalwani, Anil K ^e   Kumar, Subrinder ^d   Ploplis, Barbara ^f   Skarka, Hana ^f   Srisailapathy, C R Srikumari ^c   Wayne, Sigrid ^a   Zbar, Ross I S ^a   Verma, Ishwar C ^b   Smith, Richard J H ^a   Wilcox, Edward R ^f  

^a UNIVERSITY OF IOWA   (United States)

^b Rotary Deaf School   (India)

^c UNIVERSITY OF MADRAS   (India)

^d ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

^e Epstein Laboratories   (United States)

^f NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 9Q; COMPARATIVE STUDY; EVOKED BRAIN STEM RESPONSE; FRIEDREICH ATAXIA; GENE FREQUENCY; GENE MAPPING; GENETIC LINKAGE; HEARING IMPAIRMENT; HUMAN; PERCEPTION DEAFNESS; PERIPHERAL NERVOUS SYSTEM; PRIORITY JOURNAL; ZYGOSITY;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; CONSANGUINITY; FEMALE; GENES, RECESSIVE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; PEDIGREE;

ATAXIA; MURINAE;

EID: 0028837681     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/4.12.2391     Document Type: Article

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