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6. A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. Dinçer P, Leturcq F, Richard I, Piccolo F, Yalnizoglu D, de Toma C, Akçören Z, Broux O, Deburgrave N, Brenguier L, Roudaut C, Urtizberea JA, Jung D, Tan E, Jeanpierre M, Campbell KP, Kaplan JC, Beckmann JS, Topaloglu H. Ann Neurol; 1997 Aug; 42(2):222-9. PubMed ID: 9266733 [Abstract] [Full Text] [Related]
8. Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients. Guglieri M, Magri F, D'Angelo MG, Prelle A, Morandi L, Rodolico C, Cagliani R, Mora M, Fortunato F, Bordoni A, Del Bo R, Ghezzi S, Pagliarani S, Lucchiari S, Salani S, Zecca C, Lamperti C, Ronchi D, Aguennouz M, Ciscato P, Di Blasi C, Ruggieri A, Moroni I, Turconi A, Toscano A, Moggio M, Bresolin N, Comi GP. Hum Mutat; 2008 Feb; 29(2):258-66. PubMed ID: 17994539 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
10. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Pegoraro E, Hoffman EP. ; 1993 Oct. PubMed ID: 20301582 [Abstract] [Full Text] [Related]
11. The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12. Moreira ES, Vainzof M, Marie SK, Sertié AL, Zatz M, Passos-Bueno MR. Am J Hum Genet; 1997 Jul; 61(1):151-9. PubMed ID: 9245996 [Abstract] [Full Text] [Related]
13. The 10 autosomal recessive limb-girdle muscular dystrophies. Zatz M, de Paula F, Starling A, Vainzof M. Neuromuscul Disord; 2003 Sep; 13(7-8):532-44. PubMed ID: 12921790 [Abstract] [Full Text] [Related]
14. 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]