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47. Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. McNally EM; Passos-Bueno MR; Bönnemann CG; Vainzof M; de Sá Moreira E; Lidov HG; Othmane KB; Denton PH; Vance JM; Zatz M; Kunkel LM Am J Hum Genet; 1996 Nov; 59(5):1040-7. PubMed ID: 8900232 [TBL] [Abstract][Full Text] [Related]
52. Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene. McNally EM; Ly CT; Kunkel LM FEBS Lett; 1998 Jan; 422(1):27-32. PubMed ID: 9475163 [TBL] [Abstract][Full Text] [Related]
53. Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy. Ginjaar HB; van der Kooi AJ; Ceelie H; Kneppers AL; van Meegen M; Barth PG; Busch HF; Wokke JH; Anderson LV; Bönnemann CG; Jeanpierre M; Bolhuis PA; Moorman AF; de Visser M; Bakker E; Ommen GJ J Neurol; 2000 Jul; 247(7):524-9. PubMed ID: 10993494 [TBL] [Abstract][Full Text] [Related]
54. Deficiency of adhalin in a patient with muscular dystrophy and cardiomyopathy. McNally EM; Bönnemann CG; Kunkel LM; Bhattacharya SK N Engl J Med; 1996 Jun; 334(24):1610-1. PubMed ID: 8628353 [No Abstract] [Full Text] [Related]
55. Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster. Straub V; Duclos F; Venzke DP; Lee JC; Cutshall S; Leveille CJ; Campbell KP Am J Pathol; 1998 Nov; 153(5):1623-30. PubMed ID: 9811355 [TBL] [Abstract][Full Text] [Related]
56. Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile. Bönnemann CG; Wong J; Jones KJ; Lidov HG; Feener CA; Shapiro F; Darras BT; Kunkel LM; North KN Neuromuscul Disord; 2002 Mar; 12(3):273-80. PubMed ID: 11801399 [TBL] [Abstract][Full Text] [Related]
57. Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex. Barresi R; Moore SA; Stolle CA; Mendell JR; Campbell KP J Biol Chem; 2000 Dec; 275(49):38554-60. PubMed ID: 10993904 [TBL] [Abstract][Full Text] [Related]
58. Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan gene. Lasa A; Piccolo F; de Diego C; Jeanpierre M; Colomer J; Rodríguez MJ; Urtizberea JA; Baiget M; Kaplan J; Gallano P Eur J Hum Genet; 1998; 6(4):396-9. PubMed ID: 9781048 [TBL] [Abstract][Full Text] [Related]
59. Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin. Ljunggren A; Duggan D; McNally E; Boylan KB; Gama CH; Kunkel LM; Hoffman EP Ann Neurol; 1995 Sep; 38(3):367-72. PubMed ID: 7668821 [TBL] [Abstract][Full Text] [Related]
60. A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families. Dinçer P; Akçören Z; Demir E; Richard I; Sancak O; Kale G; Ozme S; Karaduman A; Tan E; Urtizberea JA; Beckmann JS; Topaloğlu H J Med Genet; 2000 May; 37(5):361-7. PubMed ID: 10807695 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]