A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia.

Human mutation

Volumn 16, Issue 3, 2000, Pages 277-

  Giannotti, A ^a   Tessa, A ^a   Patrono, C ^a   Florio, L D ^a   Velardo, M ^a   Dionisi Vici, C ^a   Bertini, E ^a   Santorelli, F M ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR RUNX2; TRYPTOPHAN; TUMOR PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; CLEIDOCRANIAL DYSPLASIA; GENETICS; HUMAN; ITALY; MISSENSE MUTATION;

AMINO ACID SUBSTITUTION; ARGININE; CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; HUMANS; ITALY; MUTATION, MISSENSE; NEOPLASM PROTEINS; TRANSCRIPTION FACTORS; TRYPTOPHAN;

EID: 0034267570     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200009)16:3<277::AID-HUMU25>3.0.CO;2-V     Document Type: Article

References (0)