R32W variant in Connexin 31: Mutation or polymorphism for deafness and skin disease? (multiple letters) [2]

European Journal of Human Genetics

Volumn 9, Issue 1, 2001, Pages 70-

  LoOpez Bigas N ^a   Rabionet, R ^a   Arbonees M L ^a   Estivill, X ^a   Kelsell, David ^b  

^a HOSPITAL DURAN I REYNALS   (Spain)

^b QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; ARGININE; CONNEXIN 31; DNA; GAP JUNCTION PROTEIN; UNCLASSIFIED DRUG;

CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; EVOLUTION; FAMILY; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; HEARING IMPAIRMENT; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; KERATOSIS PALMOPLANTARIS; LETTER; MOTHER; MUTATION RATE; PENETRANCE; PRIORITY JOURNAL; PROTEIN VARIANT; SKIN DISEASE; SPAIN;

EID: 84859541472     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200569     Document Type: Letter

References (0)