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12. Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects. Handa V, Mital A, Gupta M, Goyle S. Neurol India; 2001 Mar 10; 49(1):19-24. PubMed ID: 11303236 [Abstract] [Full Text] [Related]
13. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. Higuchi I, Yamada H, Fukunaga H, Iwaki H, Okubo R, Nakagawa M, Osame M, Roberds SL, Shimizu T, Campbell KP. J Clin Invest; 1994 Aug 10; 94(2):601-6. PubMed ID: 8040315 [Abstract] [Full Text] [Related]
14. Increased expression of dystrophin, beta-dystroglycan and adhalin in denervated rat muscles. Biral D, Senter L, Salviati G. J Muscle Res Cell Motil; 1996 Oct 10; 17(5):523-32. PubMed ID: 8906620 [Abstract] [Full Text] [Related]
15. 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 10; 38(3):367-72. PubMed ID: 7668821 [Abstract] [Full Text] [Related]
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 10; 10(2):243-5. PubMed ID: 7663524 [Abstract] [Full Text] [Related] Page: [Next] [New Search]