Relationship between genotype and phenotype for the CFTR gene W846X mutation.

Journal of medical genetics

Volumn 39, Issue 6, 2002, Pages

  Dugueperoux I ^a   Bellis, G ^a   Ferec C ^a   Gillet, D ^a   Scotet, V ^a   De Braekeleer, M ^a  

^a UNIVERSITÉ DE BRETAGNE OCCIDENTALE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CFTR PROTEIN, HUMAN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADOLESCENT; ADULT; ARTICLE; CHILD; CYSTIC FIBROSIS; FEMALE; GENETICS; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MALE; PHENOTYPE; POINT MUTATION;

ADOLESCENT; ADULT; CHILD; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; PHENOTYPE; POINT MUTATION;

MLCS; MLOWN;

EID: 18244424274     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.39.6.e32     Document Type: Article

References (0)