APA

Ozes B., Karagoz N., Schüle R., Rebelo A., Sobrido M., Harmuth F., Synofzik M., Pascual S. I. P., Colak M., Ciftci-Kavaklioglu B., Kara B., Ordóñez-Ugalde A., Quintáns B., Gonzalez M. A., Soysal A., Zuchner S. & Battaloglu E. (20180528). PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. : Clinical genetics.

Chicago

Ozes B, Karagoz N, Schüle R, Rebelo A, Sobrido M-J, Harmuth F, Synofzik M, Pascual S I P, Colak M, Ciftci-Kavaklioglu B, Kara B, Ordóñez-Ugalde A, Quintáns B, Gonzalez M A, Soysal A, Zuchner S and Battaloglu E. 20180528. PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. : Clinical genetics.

Harvard

Ozes B., Karagoz N., Schüle R., Rebelo A., Sobrido M., Harmuth F., Synofzik M., Pascual S. I. P., Colak M., Ciftci-Kavaklioglu B., Kara B., Ordóñez-Ugalde A., Quintáns B., Gonzalez M. A., Soysal A., Zuchner S. and Battaloglu E. (20180528). PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. : Clinical genetics.

MLA

Ozes B, Karagoz N, Schüle R, Rebelo A, Sobrido M-J, Harmuth F, Synofzik M, Pascual S I P, Colak M, Ciftci-Kavaklioglu B, Kara B, Ordóñez-Ugalde A, Quintáns B, Gonzalez M A, Soysal A, Zuchner S and Battaloglu E. PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. : Clinical genetics. 20180528.