Connexin 32 mutations from X-linked Charcot-Marie-Tooth disease patients: Functional defects and dominant negative effects

Molecular Biology of the Cell

Volumn 7, Issue 6, 1996, Pages 907-916

  Omori, Y ^a   Mesnil, M ^a   Yamasaki, H ^a  

^a INTERNATIONAL AGENCY FOR RESEARCH ON CANCER   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CHIMERIC PROTEIN; COMPLEMENTARY DNA; CYSTEINE; GAP JUNCTION PROTEIN; MESSENGER RNA; METHIONINE; MUTANT PROTEIN; PHENYLALANINE; TRYPTOPHAN; VALINE;

ARTICLE; CELL COMMUNICATION; CELL CONTACT; CELL JUNCTION; CONTROLLED STUDY; DNA TRANSFECTION; GENE MUTATION; HELA CELL; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; NONSENSE MUTATION; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; X CHROMOSOME DOMINANT DISORDER;

EID: 0029977355     PISSN: 10591524     EISSN: None     Source Type: Journal    
DOI: 10.1091/mbc.7.6.907     Document Type: Article

References (0)