Buschke-Ollendorff syndrome: Inactivating mutation of the LEMD3 gene;Syndrome de Buschke-Ollendorf: Mutation inactivatrice du gène LEMD3

Annales de Dermatologie et de Venereologie

Volumn 132, Issue 6-7 I, 2005, Pages 593-

  Dereure, O ^a  

^a HÔPITAL SAINT ELOI   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGEN; PROTEIN LEMD3; TRANSFORMING GROWTH FACTOR BETA3; UNCLASSIFIED DRUG; MEMBRANE PROTEIN;

ARTICLE; BUSCHKE OLLENDORFF SYNDROME; COLLAGEN DISEASE; ENZYME ACTIVATION; GENE FUNCTION; GENE INACTIVATION; GENE MUTATION; HUMAN; OSTEOSCLEROSIS; PHENOTYPE; GENE SILENCING; GENETICS; MUTATION;

GENE SILENCING; HUMANS; MEMBRANE PROTEINS; MUTATION; OSTEOPOIKILOSIS;

EID: 22344454202     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0151-9638(05)79351-0     Document Type: Article

References (1)

1. 3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis. Nat Genet 2004;36:1213-8.