Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene

MLA

Dieter Gläser, et al. “Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene.” Neuropediatrics, vol. 46, June 2015, pp. 282–86. 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.....5b6c0d4e3b372e1e0c2f8028ffe50e4a&authtype=sso&custid=ns315887.

APA

Dieter Gläser, Wolfgang Müller-Felber, Katharina Vill, Marius Kuhn, & Maggie C. Walter. (2015). Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene. Neuropediatrics, 46, 282–286.

Chicago

Dieter Gläser, Wolfgang Müller-Felber, Katharina Vill, Marius Kuhn, and Maggie C. Walter. 2015. “Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene.” Neuropediatrics 46 (June): 282–86. 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.....5b6c0d4e3b372e1e0c2f8028ffe50e4a&authtype=sso&custid=ns315887.