A novel mutation in TNFRSF1A associated with overlapping features of tumor necrosis factor receptor-associated periodic syndrome and hyper-IgD syndrome.

Saulsbury, F T; Remmers, E F; Aksentijevich, I

Saulsbury, F T; Remmers, E F; Aksentijevich, I.

Saulsbury FT; Department of Pediatrics, University of Virginia Health System, Charlottesville, Virginia 22908, USA. fts@virginia.edu

Clin Exp Rheumatol ; 28(1): 94-6, 2010.

Article en En | MEDLINE | ID: mdl-20346247

Asunto(s)

Fiebre Mediterránea Familiar/genética; Deficiencia de Mevalonato Quinasa/genética; Receptores Tipo I de Factores de Necrosis Tumoral/genética; Receptores del Factor de Necrosis Tumoral/genética; Niño; Humanos; Masculino; Mutación Puntual

Search on Google

Imprimir

XML

PubMed Links

Banco de datos: MEDLINE Asunto principal: Fiebre Mediterránea Familiar / Receptores del Factor de Necrosis Tumoral / Receptores Tipo I de Factores de Necrosis Tumoral / Deficiencia de Mevalonato Quinasa Tipo de estudio: Risk_factors_studies Límite: Child / Humans / Male Idioma: En Año: 2010 Tipo del documento: Article

Search on Google

Imprimir

XML

PubMed Links