S. Britton

Dysferlin is a plasma membrane protein and is expressed early in human development.

K. Bushby, M. Johnson, F. Fougerousse, 1999, Human molecular genetics.

The third human FER-1-like protein is highly similar to dysferlin.

K. Bushby, T. Freeman, R. Bashir, 2000, Genomics.

Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy

J. Beckmann, K. Bushby, J. Oeltjen, 2001, Neurology.

A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

J. Beckmann, K. Bushby, M. Lako, 1998, Nature Genetics.

Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).

C. Greenberg, T. Weiler, R. Bashir, 1999, Human molecular genetics.

The molecular biology of LGMD2B — Towards the identification of the LGMD gene on chromosome 2p13

K. Bushby, T. Strachan, M. Passos-Bueno, 1996, Neuromuscular Disorders.

Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy

N. Bourg, R. Barohn, D. McKenna-Yasek, 2001, Neurology.