Is CFTR 621+3 A>G a cystic fibrosis causing mutation?
スポンサーリンク
概要
- 論文の詳細を見る
- Nature Publishing Groupの論文
- 2010-01-01
著者
-
Pertegato Vanessa
Clinical Genetics Unit Department Of Pediatrics University Of Padova
-
FORZAN Monica
Clinical Genetics Unit, Department of Pediatrics, University of Padova
-
SALVIATI Leonardo
Clinical Genetics Unit, Department of Pediatrics, University of Padova
-
CASARIN Alberto
Clinical Genetics Unit, Department of Pediatrics, University of Padova
-
BRUSON Alice
Clinical Genetics Unit, Department of Pediatrics, University of Padova
-
TREVISSON Eva
Clinical Genetics Unit, Department of Pediatrics, University of Padova
-
DI GIANANTONIO
Clinical Genetics Unit, Department of Pediatrics, University of Padova
-
CLEMENTI Maurizio
Clinical Genetics Unit, Department of Pediatrics, University of Padova
-
Bruson Alice
Clinical Genetics Unit Department Of Pediatrics University Of Padova
-
Forzan Monica
Clinical Genetics Unit Department Of Pediatrics University Of Padova
-
Di Gianantonio
Clinical Genetics Unit Department Of Pediatrics University Of Padova
-
Casarin Alberto
Clinical Genetics Unit Department Of Pediatrics University Of Padova
-
Salviati Leonardo
Clinical Genetics Unit Department Of Pediatrics University Of Padova
-
Salviati Leonardo
Clinical Genetics Unit And Hematology-oncology Laboratory Department Of Pediatrics University Of Padova
-
Clementi Maurizio
Clinical Genetics Unit Department Of Pediatrics University Of Padova
-
Trevisson Eva
Clinical Genetics Unit and Hematology-Oncology Laboratory, Department of Pediatrics, University of Padova
関連論文
- Is CFTR 621+3 A>G a cystic fibrosis causing mutation?
- Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiency