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9. Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene. Nakagawa M; Matsuzaki T; Suehara M; Kanzato N; Takashima H; Higuchi I; Matsumura T; Goto K; Arahata K; Osame M J Neurol Sci; 2001 Feb; 184(1):15-9. PubMed ID: 11231027 [TBL] [Abstract][Full Text] [Related]
10. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Liu J; Aoki M; Illa I; Wu C; Fardeau M; Angelini C; Serrano C; Urtizberea JA; Hentati F; Hamida MB; Bohlega S; Culper EJ; Amato AA; Bossie K; Oeltjen J; Bejaoui K; McKenna-Yasek D; Hosler BA; Schurr E; Arahata K; de Jong PJ; Brown RH Nat Genet; 1998 Sep; 20(1):31-6. PubMed ID: 9731526 [TBL] [Abstract][Full Text] [Related]
11. Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation. McNally EM; Ly CT; Rosenmann H; Mitrani Rosenbaum S; Jiang W; Anderson LV; Soffer D; Argov Z Am J Med Genet; 2000 Apr; 91(4):305-12. PubMed ID: 10766988 [TBL] [Abstract][Full Text] [Related]
13. A new dysferlin gene mutation in two Japanese families with limb-girdle muscular dystrophy 2B and Miyoshi myopathy. Ueyama H; Kumamoto T; Nagao S; Masuda T; Horinouchi H; Fujimoto S; Tsuda T Neuromuscul Disord; 2001 Mar; 11(2):139-45. PubMed ID: 11257469 [TBL] [Abstract][Full Text] [Related]
14. Dysferlinopathy: a clinical and histopathological study of 28 patients from India. Nalini A; Gayathri N Neurol India; 2008; 56(3):379-85; discussion 386-7. PubMed ID: 18974568 [TBL] [Abstract][Full Text] [Related]