Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family.

European journal of human genetics : EJHG

Volumn 8, Issue 6, 2000, Pages 469-472

  Kelsell, D P ^a   Wilgoss, A L ^a   Richard, G ^a   Stevens, H P ^a   Munro, C S ^a   Leigh, I M ^a  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN; GJB3 PROTEIN, HUMAN;

ARTICLE; FEMALE; GENETICS; HEARING IMPAIRMENT; HETERODUPLEX ANALYSIS; HUMAN; KERATOSIS PALMOPLANTARIS; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; POINT MUTATION;

CONNEXINS; DEAFNESS; DNA MUTATIONAL ANALYSIS; FEMALE; HETERODUPLEX ANALYSIS; HUMANS; KERATODERMA, PALMOPLANTAR; MALE; MUTATION; PEDIGREE; POINT MUTATION;

EID: 0034198467     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)