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Journal Abstract Search

361 related items for PubMed ID: 9266733

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  • 5. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
    Nigro V, de Sá Moreira E, Piluso G, Vainzof M, Belsito A, Politano L, Puca AA, Passos-Bueno MR, Zatz M.
    Nat Genet; 1996 Oct; 14(2):195-8. PubMed ID: 8841194
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  • 8. Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD.
    Passos-Bueno MR, Moreira ES, Vainzof M, Marie SK, Zatz M.
    Hum Mol Genet; 1996 Jun; 5(6):815-20. PubMed ID: 8776597
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  • 9. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.
    Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M.
    Hum Mol Genet; 1995 Jul; 4(7):1163-7. PubMed ID: 8528203
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  • 10. Understanding the heterogeneity of the limb-girdle muscular dystrophies.
    Bushby K.
    Biochem Soc Trans; 1996 May; 24(2):489-96. PubMed ID: 8736790
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  • 11. Novel mutations in three patients with LGMD2C with phenotypic differences.
    Vermeer S, Verrips A, Willemsen MA, ter Laak HJ, Ginjaar IB, Hamel BC.
    Pediatr Neurol; 2004 Apr; 30(4):291-4. PubMed ID: 15087111
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  • 12. Molecular diagnosis and counseling in a family presenting compound heterozygosity for autosomal recessive limb-girdle muscular dystrophy.
    Dos Santos MR, Vieira EM, Reis Lima M.
    Genet Couns; 2001 Apr; 12(3):223-9. PubMed ID: 11693784
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  • 14. [Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family].
    Horváth R, Walter MC, Lochmüller H, Hübner A, Karcagi V, Pikó H, Timár L, Komoly S.
    Ideggyogy Sz; 2005 Jan 20; 58(1-2):52-8. PubMed ID: 15884399
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  • 15. Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).
    Carrié A, Piccolo F, Leturcq F, de Toma C, Azibi K, Beldjord C, Vallat JM, Merlini L, Voit T, Sewry C, Urtizberea JA, Romero N, Tomé FM, Fardeau M, Sunada Y, Campbell KP, Kaplan JC, Jeanpierre M.
    J Med Genet; 1997 Jun 20; 34(6):470-5. PubMed ID: 9192266
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  • 16. Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene.
    Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Poleshchuk VV, Markova ED, Tsuji S.
    Genomics; 1997 Jun 01; 42(2):345-8. PubMed ID: 9192858
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  • 19. Specific assembly pathway of sarcoglycans is dependent on beta- and delta-sarcoglycan.
    Shi W, Chen Z, Schottenfeld J, Stahl RC, Kunkel LM, Chan YM.
    Muscle Nerve; 2004 Mar 01; 29(3):409-19. PubMed ID: 14981741
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  • 20. Molecular bases of autosomal recessive limb-girdle muscular dystrophies.
    Nigro V.
    Acta Myol; 2003 Sep 01; 22(2):35-42. PubMed ID: 14959561
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