APA

Doe J., Kaindl A. M., Jijiwa M., de la Vega M., Hu H., Griffiths G. S., Fontelonga T. M., Barraza P., Cruz V., Van Ry P., Ramos J. W., Burkin D. J. & Matter M. L. (20170515). PTRH2 gene mutation causes progressive congenital skeletal muscle pathology. : Human molecular genetics.

Chicago

Doe Jinger, Kaindl Angela M, Jijiwa Mayumi, de la Vega Michelle, Hu Hao, Griffiths Genevieve S, Fontelonga Tatiana M, Barraza Pamela, Cruz Vivian, Van Ry Pam, Ramos Joe W, Burkin Dean J and Matter Michelle L. 20170515. PTRH2 gene mutation causes progressive congenital skeletal muscle pathology. : Human molecular genetics.

Harvard

Doe J., Kaindl A. M., Jijiwa M., de la Vega M., Hu H., Griffiths G. S., Fontelonga T. M., Barraza P., Cruz V., Van Ry P., Ramos J. W., Burkin D. J. and Matter M. L. (20170515). PTRH2 gene mutation causes progressive congenital skeletal muscle pathology. : Human molecular genetics.

MLA

Doe Jinger, Kaindl Angela M, Jijiwa Mayumi, de la Vega Michelle, Hu Hao, Griffiths Genevieve S, Fontelonga Tatiana M, Barraza Pamela, Cruz Vivian, Van Ry Pam, Ramos Joe W, Burkin Dean J and Matter Michelle L. PTRH2 gene mutation causes progressive congenital skeletal muscle pathology. : Human molecular genetics. 20170515.