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5. A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21. Tétreault M; Duquette A; Thiffault I; Bherer C; Jarry J; Loisel L; Banwell B; D'Anjou G; Mathieu J; Robitaille Y; Vanasse M; Brais B Brain; 2006 Aug; 129(Pt 8):2077-84. PubMed ID: 16760198 [TBL] [Abstract][Full Text] [Related]
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8. Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J. Udd B; Vihola A; Sarparanta J; Richard I; Hackman P Neurology; 2005 Feb; 64(4):636-42. PubMed ID: 15728284 [TBL] [Abstract][Full Text] [Related]
9. Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes. Fendri K; Kefi M; Hentati F; Amouri R Neuromuscul Disord; 2006 May; 16(5):316-20. PubMed ID: 16616845 [TBL] [Abstract][Full Text] [Related]
10. Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients. Kley RA; Hellenbroich Y; van der Ven PF; Fürst DO; Huebner A; Bruchertseifer V; Peters SA; Heyer CM; Kirschner J; Schröder R; Fischer D; Müller K; Tolksdorf K; Eger K; Germing A; Brodherr T; Reum C; Walter MC; Lochmüller H; Ketelsen UP; Vorgerd M Brain; 2007 Dec; 130(Pt 12):3250-64. PubMed ID: 18055494 [TBL] [Abstract][Full Text] [Related]
11. Clinical and magnetic resonance imaging features of 'diamond on quadriceps' sign in dysferlinopathy. Pradhan S Neurol India; 2009; 57(2):172-5. PubMed ID: 19439848 [TBL] [Abstract][Full Text] [Related]
12. Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutation. Harel T; Goldberg Y; Shalev SA; Chervinski I; Ofir R; Birk OS Eur J Hum Genet; 2004 Jan; 12(1):38-43. PubMed ID: 14523375 [TBL] [Abstract][Full Text] [Related]
13. Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy. Müller JS; Piko H; Schoser BG; Schlotter-Weigel B; Reilich P; Gürster S; Born C; Karcagi V; Pongratz D; Lochmüller H; Walter MC Neuromuscul Disord; 2006 Jul; 16(7):432-6. PubMed ID: 16730439 [TBL] [Abstract][Full Text] [Related]
14. Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5. Penttilä S; Palmio J; Suominen T; Raheem O; Evilä A; Muelas Gomez N; Tasca G; Waddell LB; Clarke NF; Barboi A; Hackman P; Udd B Neurology; 2012 Mar; 78(12):897-903. PubMed ID: 22402862 [TBL] [Abstract][Full Text] [Related]
15. The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations. Frosk P; Greenberg CR; Tennese AA; Lamont R; Nylen E; Hirst C; Frappier D; Roslin NM; Zaik M; Bushby K; Straub V; Zatz M; de Paula F; Morgan K; Fujiwara TM; Wrogemann K Hum Mutat; 2005 Jan; 25(1):38-44. PubMed ID: 15580560 [TBL] [Abstract][Full Text] [Related]
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17. A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus. Weiler T; Greenberg CR; Zelinski T; Nylen E; Coghlan G; Crumley MJ; Fujiwara TM; Morgan K; Wrogemann K Am J Hum Genet; 1998 Jul; 63(1):140-7. PubMed ID: 9634523 [TBL] [Abstract][Full Text] [Related]
18. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles. Nakamura A; Yoshida K; Ikeda S Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303 [TBL] [Abstract][Full Text] [Related]