Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiency
スポンサーリンク
概要
- 論文の詳細を見る
- Nature Publishing Groupの論文
- 2009-07-01
著者
-
TREVISSON Eva
Clinical Genetics Unit, Department of Pediatrics, University of Padova
-
Salviati Leonardo
Clinical Genetics Unit And Hematology-oncology Laboratory Department Of Pediatrics University Of Padova
-
SACCONI Sabrina
Centre de Reference des Maladies Neuromusculaires et CNRS UMR 6543, Faculte de Medicine, Universite de Nice
-
Sacconi Sabrina
Centre De Reference Des Maladies Neuromusculaires Et Cnrs Umr 6543 Faculte De Medicine Universite De Nice
-
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