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Pubmed for Handhelds

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Journal Abstract Search

157 related items for PubMed ID: 8866424

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  • 3. [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; 45(2):136-40. PubMed ID: 9120997
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  • 4. 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
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  • 5. [The frequency of patients with adhalin deficiency in a muscular dystrophy patient population].
    Hayashi YK, Arahata K.
    Nihon Rinsho; 1997 Dec; 55(12):3165-8. PubMed ID: 9436429
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  • 6. Sarcoglycans in muscular dystrophy.
    Hack AA, Groh ME, McNally EM.
    Microsc Res Tech; 1997 Dec; 48(3-4):167-80. PubMed ID: 10679964
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  • 7. Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex.
    Duggan DJ, Hoffman EP.
    Neuromuscul Disord; 1996 Dec; 6(6):475-82. PubMed ID: 9027858
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  • 9. Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle.
    Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Suzuki A, Hagiwara Y, Hayashi YK, Arahata K, Nonaka I, Hirai S.
    Biochem Biophys Res Commun; 1994 Sep 15; 203(2):979-83. PubMed ID: 8093083
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  • 10. Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).
    Bönnemann CG, Passos-Bueno MR, McNally EM, Vainzof M, de Sá Moreira E, Marie SK, Pavanello RC, Noguchi S, Ozawa E, Zatz M, Kunkel LM.
    Hum Mol Genet; 1996 Dec 15; 5(12):1953-61. PubMed ID: 8968749
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  • 12. Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.
    Araishi K, Sasaoka T, Imamura M, Noguchi S, Hama H, Wakabayashi E, Yoshida M, Hori T, Ozawa E.
    Hum Mol Genet; 1999 Sep 15; 8(9):1589-98. PubMed ID: 10441321
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  • 16. [Adhalin gene mutations in malignant limb-girdle muscular dystrophy and clinical features in adhalin-deficient muscular dystrophy].
    Endo T, Akaike M, Kawai H, Matsumura K, Saito S.
    Rinsho Shinkeigaku; 1996 Mar 15; 36(3):415-22. PubMed ID: 8741343
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  • 20. [Clinicopathological characteristics and molecular genetics of adhalin deficiency (severe childhood autosomal recessive muscular dystrophy/SCARMD)].
    Matsumura K.
    Nihon Rinsho; 1997 Dec 15; 55(12):3154-8. PubMed ID: 9436427
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