Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia.

Circulation research

Volumn 96, Issue 10, 2005, Pages

  Shibayama, Junko ^a   Paznekas, William ^a   Seki, Akiko ^a   Taffet, Steven ^a   Jabs, Ethylin Wang ^a   Delmar, Mario ^a   Musa, Hassan ^a  

^a State University of New York Upstate Medical University: College of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 43;

ARTICLE; CELL COMMUNICATION; CELL JUNCTION; CHEMISTRY; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; EYE MALFORMATION; GENETICS; HELA CELL; HUMAN; MULTIPLE MALFORMATION SYNDROME; MUTATION; PHYSIOLOGY; TOOTH MALFORMATION;

ABNORMALITIES, MULTIPLE; CELL COMMUNICATION; CONNEXIN 43; CRANIOFACIAL ABNORMALITIES; EYE ABNORMALITIES; GAP JUNCTIONS; HEART DEFECTS, CONGENITAL; HELA CELLS; HUMANS; MUTATION; TOOTH ABNORMALITIES;

MLCS; MLOWN;

EID: 23744507557     PISSN: None     EISSN: 15244571     Source Type: Journal    
DOI: 10.1161/01.res.0000168369.79972.d2     Document Type: Article

References (0)