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Journal Abstract Search
216 related items for PubMed ID: 7668821
21. [Adhalin(alpha-sarcoglycan) gene mutations in patients with malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi)]. Endo T, Kawai H. Nihon Rinsho; 1997 Dec; 55(12):3159-64. PubMed ID: 9436428 [Abstract] [Full Text] [Related]
22. 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 [Abstract] [Full Text] [Related]
25. Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries. Fardeau M, Matsumura K, Tomé FM, Collin H, Leturcq F, Kaplan JC, Campbell KP. C R Acad Sci III; 1993 Aug; 316(8):799-804. PubMed ID: 8044705 [Abstract] [Full Text] [Related]
28. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy. Roberds SL, Leturcq F, Allamand V, Piccolo F, Jeanpierre M, Anderson RD, Lim LE, Lee JC, Tomé FM, Romero NB. Cell; 1994 Aug 26; 78(4):625-33. PubMed ID: 8069911 [Abstract] [Full Text] [Related]
30. The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin. Hayashi YK, Mizuno Y, Yoshida M, Nonaka I, Ozawa E, Arahata K. Neurology; 1995 Mar 26; 45(3 Pt 1):551-4. PubMed ID: 7898714 [Abstract] [Full Text] [Related]
36. A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotype. Goldberg LR, Hausmanowa-Petrusewicz I, Fidzianska A, Duggan DJ, Steinberg LS, Hoffman EP. Ann Neurol; 1998 Dec 26; 44(6):971-6. PubMed ID: 9851445 [Abstract] [Full Text] [Related]