Connexin mutations in skin disease and hearing loss

American Journal of Human Genetics

Volumn 68, Issue 3, 2001, Pages 559-568

  Kelsell, David P ^a   Di, Wei Li ^a   Houseman, Mark J ^b  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^b ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GAP JUNCTION PROTEIN;

AUTOSOMAL RECESSIVE DISORDER; FAMILY STUDY; FRAMESHIFT MUTATION; GAP JUNCTION; GENE MAPPING; GENE MUTATION; GENODERMATOSIS; HEARING LOSS; HUMAN; KERATODERMA; MISSENSE MUTATION; PRIORITY JOURNAL; REVIEW; SKIN DISEASE;

EID: 0035096676     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/318803     Document Type: Article

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