APA

Ormazabal A., Serrano M., Garcia-Cazorla A., Campistol J., Artuch R., Castro de Castro P., Barredo-Valderrama E., Armstrong J., Toma C. & Cormand B. (20120229). Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype. : Movement disorders : official journal of the Movement Disorder Society.

Chicago

Ormazabal Aida, Serrano Mercedes, Garcia-Cazorla Angels, Campistol Jaume, Artuch Rafael, Castro de Castro Pedro, Barredo-Valderrama Estíbaliz, Armstrong Judith, Toma Claudio and Cormand Bru. 20120229. Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype. : Movement disorders : official journal of the Movement Disorder Society.

Harvard

Ormazabal A., Serrano M., Garcia-Cazorla A., Campistol J., Artuch R., Castro de Castro P., Barredo-Valderrama E., Armstrong J., Toma C. and Cormand B. (20120229). Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype. : Movement disorders : official journal of the Movement Disorder Society.

MLA

Ormazabal Aida, Serrano Mercedes, Garcia-Cazorla Angels, Campistol Jaume, Artuch Rafael, Castro de Castro Pedro, Barredo-Valderrama Estíbaliz, Armstrong Judith, Toma Claudio and Cormand Bru. Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype. : Movement disorders : official journal of the Movement Disorder Society. 20120229.