Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes

MLA

Jean-Michel Vallat, et al. “Novel Mutations in the PRX and the MTMR2 Genes Are Responsible for Unusual Charcot-Marie-Tooth Disease Phenotypes.” Neuromuscular Disorders : NMD, vol. 21, no. 8, Mar. 2011. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....1a83fc0d42e731862feee445799d8ebb&authtype=sso&custid=ns315887.

APA

Jean-Michel Vallat, Rafaëlle Bernard, D. Grid, Tarik Hamadouche, Nora Bellatache, Benoît Funalot, Meriem Tazir, Nicolas Lévy, Sonia Nouioua, Radia Bouderba, S. Assami, & Traki Benhassine. (2011). Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. Neuromuscular Disorders : NMD, 21(8).

Chicago

Jean-Michel Vallat, Rafaëlle Bernard, D. Grid, Tarik Hamadouche, Nora Bellatache, Benoît Funalot, Meriem Tazir, et al. 2011. “Novel Mutations in the PRX and the MTMR2 Genes Are Responsible for Unusual Charcot-Marie-Tooth Disease Phenotypes.” Neuromuscular Disorders : NMD 21 (8). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....1a83fc0d42e731862feee445799d8ebb&authtype=sso&custid=ns315887.