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Journal Abstract Search

179 related items for PubMed ID: 9646269

  • 1. [Muscular dystrophy due to a mutation in the gene of alpha-sarcoglycan subunit of dystrophin associated protein complex].
    Urtasun M, Poza JJ, Gallano P, Lasa A, Sáenz A, Cobo AM, Leturcq F, López de Munain A, García-Bragado F.
    Med Clin (Barc); 1998 Apr 25; 110(14):538-42. PubMed ID: 9646269
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  • 2. [Gene analysis in patients with muscular dystrophy: alpha-sarcoglycan (adhalin) gene mutations in patients with malignant limb-girdle muscular dystrophy].
    Akaike M, Kawai H.
    Rinsho Byori; 1997 Feb 25; 45(2):136-40. PubMed ID: 9120997
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  • 3. [The frequency of patients with adhalin deficiency in a muscular dystrophy patient population].
    Hayashi YK, Arahata K.
    Nihon Rinsho; 1997 Dec 25; 55(12):3165-8. PubMed ID: 9436429
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  • 4. Sarcoglycans in muscular dystrophy.
    Hack AA, Groh ME, McNally EM.
    Microsc Res Tech; 1997 Dec 25; 48(3-4):167-80. PubMed ID: 10679964
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  • 8. [Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation].
    Eirís-Puñal J, Pintos-Martínez E, Lasa A, Gallano P, Castro-Gago M.
    Rev Neurol; 1997 Dec 25; 34(5):486-9. PubMed ID: 12040521
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  • 11. 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 13; 334(24):1610-1. PubMed ID: 8628353
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  • 19. Absence of alpha-sarcoglycan and novel missense mutations in the alpha-sarcoglycan gene in a young British girl with muscular dystrophy.
    Quinlivan RM, Robb SA, Sewry C, Dubowitz V, Piccolo F, Kaplan JC.
    Dev Med Child Neurol; 1997 Nov 13; 39(11):770-4. PubMed ID: 9393893
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  • 20. Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity.
    Piccolo F, Roberds SL, Jeanpierre M, Leturcq F, Azibi K, Beldjord C, Carrié A, Récan D, Chaouch M, Reghis A.
    Nat Genet; 1995 Jun 13; 10(2):243-5. PubMed ID: 7663524
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