Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms.

Autor:	Cheillan, David1, Joncquel-Chevalier Curt, Marie2, Briand, Gilbert2,3, Salomons, Gajja S.4, Mention-Mulliez, Karine5, Dobbelaere, Dries5, Cuisset, Jean-Marie6, Lion-Fran‡ois, Laurence7, Des Portes, Vincent7, Chabli, Allel8, Valayannopoulos, Vassili9, Benoist, Jean-Fran‡ois10, Pinard, Jean-Marc11, Simard, Gilles12, Douay, Olivier12, Deiva, Kumaran13, Afenjar, Alexandra14, H‚ron, Delphine15, Rivier, Fran‡ois16, Chabrol, Brigitte17
Zdroj:	Orphanet Journal of Rare Diseases. 2012, Vol. 7 Issue 1, p96-105. 10p. 3 Charts.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu