Identification and characterization of a novel splice-site mutation in a patient with Wiskott-Aldrich syndrome
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2003-11-01
著者
-
Carreras Carmen
Unidad De Hematologia Infantil Hospital Universitari" La Fe
-
ANDREU Nuria
Programa Gens i Malatia, Centre de Regulacio Genomica
-
PRIETO Felix
Unidad de Genetica, Hospital Universitari "La Fe"
-
ESTIVILL Xavier
Programa Gens i Malaltia, Centre de Regulacio Genomica
-
VOLPINI Victor
Centre de Genetica Medica i Molecular-IRO, L'Hospitalet de Llobregat
-
FILLAT Cristina
Programa Gens i Malatia, Centre de Regulacio Genomica
-
Prieto Felix
Unidad De Genetica Hospital Universitari "la Fe
-
Andreu Nuria
Programa Gens I Malatia Centre De Regulacio Genomica
-
Estivill Xavier
Programa Gens I Malaltia Centre De Regulacio Genomica
-
Fillat Cristina
Programa Gens I Malatia Centre De Regulacio Genomica
-
Volpini Victor
Centre De Genetica Medica I Molecular-iro L'hospitalet De Llobregat
-
Andreu Nuria
Programa Gens i Malaltia, Centre de Regulacio Genomica-CRG-UPF
-
Volpini Victor
Centre de Diagnosi Genetic Molecular-IRO-IDIBELL, L'Hospitalet de Llobregat
-
FILLAT Cristina
Programa Gens i Malaltia, Centre de Regulacio Genomica-CRG-UPF
関連論文
- Identification and characterization of a novel splice-site mutation in a patient with Wiskott-Aldrich syndrome
- A novel Wiskott-Aldrich syndrome protein (WASP) complex mutation identified in a WAS patient results in an aberrant product at the C-terminus from two transcripts with unusual polyA signals