APA

Weedon M. N., Hastings R., Caswell R., Xie W., Paszkiewicz K., Antoniadi T., Williams M., King C., Greenhalgh L., Newbury-Ecob R. & Ellard S. (20111010). Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease. : American journal of human genetics.

Chicago

Weedon Michael N, Hastings Robert, Caswell Richard, Xie Weijia, Paszkiewicz Konrad, Antoniadi Thalia, Williams Maggie, King Cath, Greenhalgh Lynn, Newbury-Ecob Ruth and Ellard Sian. 20111010. Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease. : American journal of human genetics.

Harvard

Weedon M. N., Hastings R., Caswell R., Xie W., Paszkiewicz K., Antoniadi T., Williams M., King C., Greenhalgh L., Newbury-Ecob R. and Ellard S. (20111010). Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease. : American journal of human genetics.

MLA

Weedon Michael N, Hastings Robert, Caswell Richard, Xie Weijia, Paszkiewicz Konrad, Antoniadi Thalia, Williams Maggie, King Cath, Greenhalgh Lynn, Newbury-Ecob Ruth and Ellard Sian. Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease. : American journal of human genetics. 20111010.