APA

Weiler T., Bashir R., Anderson L. V., Davison K., Moss J. A., Britton S., Nylen E., Keers S., Vafiadaki E., Greenberg C. R., Bushby C. R. & Wrogemann K. (19990623). Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s). : Human molecular genetics.

Chicago

Weiler T, Bashir R, Anderson L V, Davison K, Moss J A, Britton S, Nylen E, Keers S, Vafiadaki E, Greenberg C R, Bushby C R and Wrogemann K. 19990623. Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s). : Human molecular genetics.

Harvard

Weiler T., Bashir R., Anderson L. V., Davison K., Moss J. A., Britton S., Nylen E., Keers S., Vafiadaki E., Greenberg C. R., Bushby C. R. and Wrogemann K. (19990623). Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s). : Human molecular genetics.

MLA

Weiler T, Bashir R, Anderson L V, Davison K, Moss J A, Britton S, Nylen E, Keers S, Vafiadaki E, Greenberg C R, Bushby C R and Wrogemann K. Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s). : Human molecular genetics. 19990623.