APA

Schormair B., Kemlink D., Mollenhauer B., Fiala O., Machetanz G., Roth J., Berutti R., Strom T. M., Haslinger B., Trenkwalder C., Zahorakova D., Martasek P., Ruzicka E. & Winkelmann J. (20190911). Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease. : Clinical genetics.

Chicago

Schormair B, Kemlink D, Mollenhauer B, Fiala O, Machetanz G, Roth J, Berutti R, Strom T M, Haslinger B, Trenkwalder C, Zahorakova D, Martasek P, Ruzicka E and Winkelmann J. 20190911. Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease. : Clinical genetics.

Harvard

Schormair B., Kemlink D., Mollenhauer B., Fiala O., Machetanz G., Roth J., Berutti R., Strom T. M., Haslinger B., Trenkwalder C., Zahorakova D., Martasek P., Ruzicka E. and Winkelmann J. (20190911). Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease. : Clinical genetics.

MLA

Schormair B, Kemlink D, Mollenhauer B, Fiala O, Machetanz G, Roth J, Berutti R, Strom T M, Haslinger B, Trenkwalder C, Zahorakova D, Martasek P, Ruzicka E and Winkelmann J. Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease. : Clinical genetics. 20190911.