APA

Shayota B. J., Soler-Alfonso C., Bekheirnia M. R., Mizerik E., Boyer S. W., Xiao R., Yang Y., Elsea S. H. & Scaglia F. (20200421). Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency. : American journal of medical genetics. Part A.

Chicago

Shayota Brian J, Soler-Alfonso Claudia, Bekheirnia Mir Reza, Mizerik Elizabeth, Boyer Suzy W, Xiao Rui, Yang Yaping, Elsea Sarah H and Scaglia Fernando. 20200421. Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency. : American journal of medical genetics. Part A.

Harvard

Shayota B. J., Soler-Alfonso C., Bekheirnia M. R., Mizerik E., Boyer S. W., Xiao R., Yang Y., Elsea S. H. and Scaglia F. (20200421). Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency. : American journal of medical genetics. Part A.

MLA

Shayota Brian J, Soler-Alfonso Claudia, Bekheirnia Mir Reza, Mizerik Elizabeth, Boyer Suzy W, Xiao Rui, Yang Yaping, Elsea Sarah H and Scaglia Fernando. Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency. : American journal of medical genetics. Part A. 20200421.