APA
Cheillan D., Joncquel-Chevalier Curt M., Briand G., Salomons G. S., Mention-Mulliez K., Dobbelaere D., Cuisset J., Lion-François L., Portes V. D., Chabli A., Valayannopoulos V., Benoist J., Pinard J., Simard G., Douay O., Deiva K., Afenjar A., Héron D., Rivier F., Chabrol B., Prieur F., Cartault F., Pitelet G., Goldenberg A., Bekri S., Gerard M., Delorme R., Tardieu M., Porchet N., Vianey-Saban C. & Vamecq J. (20130621). Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms. : Orphanet journal of rare diseases.
Chicago
Cheillan David, Joncquel-Chevalier Curt Marie, Briand Gilbert, Salomons Gajja S, Mention-Mulliez Karine, Dobbelaere Dries, Cuisset Jean-Marie, Lion-François Laurence, Portes Vincent Des, Chabli Allel, Valayannopoulos Vassili, Benoist Jean-François, Pinard Jean-Marc, Simard Gilles, Douay Olivier, Deiva Kumaran, Afenjar Alexandra, Héron Delphine, Rivier François, Chabrol Brigitte, Prieur Fabienne, Cartault François, Pitelet Gaëlle, Goldenberg Alice, Bekri Soumeya, Gerard Marion, Delorme Richard, Tardieu Marc, Porchet Nicole, Vianey-Saban Christine and Vamecq Joseph. 20130621. Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms. : Orphanet journal of rare diseases.
Harvard
Cheillan D., Joncquel-Chevalier Curt M., Briand G., Salomons G. S., Mention-Mulliez K., Dobbelaere D., Cuisset J., Lion-François L., Portes V. D., Chabli A., Valayannopoulos V., Benoist J., Pinard J., Simard G., Douay O., Deiva K., Afenjar A., Héron D., Rivier F., Chabrol B., Prieur F., Cartault F., Pitelet G., Goldenberg A., Bekri S., Gerard M., Delorme R., Tardieu M., Porchet N., Vianey-Saban C. and Vamecq J. (20130621). Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms. : Orphanet journal of rare diseases.
MLA
Cheillan David, Joncquel-Chevalier Curt Marie, Briand Gilbert, Salomons Gajja S, Mention-Mulliez Karine, Dobbelaere Dries, Cuisset Jean-Marie, Lion-François Laurence, Portes Vincent Des, Chabli Allel, Valayannopoulos Vassili, Benoist Jean-François, Pinard Jean-Marc, Simard Gilles, Douay Olivier, Deiva Kumaran, Afenjar Alexandra, Héron Delphine, Rivier François, Chabrol Brigitte, Prieur Fabienne, Cartault François, Pitelet Gaëlle, Goldenberg Alice, Bekri Soumeya, Gerard Marion, Delorme Richard, Tardieu Marc, Porchet Nicole, Vianey-Saban Christine and Vamecq Joseph. Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms. : Orphanet journal of rare diseases. 20130621.