Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy

MLA

Nguyen, M.(Minh), et al. Pathogenic CWF19L1 Variants as a Novel Cause of Autosomal Recessive Cerebellar Ataxia and Atrophy. 2016. 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=edsoai&AN=edsoai.on1019672451&authtype=sso&custid=ns315887.

APA

Nguyen, M. (Minh), Boesten, I. (Iris), Hellebrekers, D. M. E. I. (Debby), Vanoevelen, J. (Jo), Kamps, R. (Rick), De Koning, B. (Bart), Coo, I. F. M. (René) de, Gerards, M. (Mike), & Smeets, H. J. M. (Hubert). (2016). Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy.

Chicago

Nguyen, M. (Minh), I. (Iris) Boesten, D.M.E.I. (Debby) Hellebrekers, J. (Jo) Vanoevelen, R. (Rick) Kamps, B. (Bart) De Koning, I.F.M. (René) de Coo, M. (Mike) Gerards, and H.J.M. (Hubert) Smeets. 2016. “Pathogenic CWF19L1 Variants as a Novel Cause of Autosomal Recessive Cerebellar Ataxia and Atrophy.” 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=edsoai&AN=edsoai.on1019672451&authtype=sso&custid=ns315887.