Citations for
1LGMD2F, SGCD
Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?
Bauer R, Hudson J, Müller HD, Sommer C, Dekomien G, Bourke J, Routledge D, Bushby K, Klepper J, Straub V.
Eur J Hum Genet 17(9):1148-53. Epub 2009 Mar 4.PMID: 19259135 2009
2LGMD2C, LGMD2D, LGMD2E, LGMD2F, SGCA, SGCB, SGCD, SGCG
Revised spectrum of mutations in sarcoglycanopathies.
Trabelsi M, Kavian N, Daoud F, Commere V, Deburgrave N, Beugnet C, Llense S, Barbot JC, Vasson A, Kaplan JC, Leturcq F, Chelly J.
Eur J Hum Genet 16(7):793-803. Epub 2008 Feb 20. 2008
3WDHD1, CABP2, CEBPZ, DOCK2, NPFFR2, KLRB1, MMP24, PPM1G, SGCD, SLC4A8
Human-specific subfamilies of HERV-K (HML-2) long terminal repeats: three master genes were active simultaneously during branching of hominoid lineages( small star, filled )
Buzdin A, Ustyugova S, Khodosevich K, Mamedov I, Lebedev Y, Hunsmann G, Sverdlov E.
Genomics 81(2):149-56. 2003
4CMD1L, LGMD2F, SGCD, TAZ
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy.
Tsubata S, Bowles KR, Vatta M, Zintz C, Titus J, Muhonen L, Bowles NE, Towbin JA.
J Clin Invest 106(5):655-62. 2000
5SGCA, SGCD, SSPN
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy.
Coral-Vazquez R, et al.
Cell 98(4):465-74. 1999
6SGCD, LGMD2F
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2).
Duggan DJ, et al.
Neurogenetics 1 : 49-58. 1997
7SGCD
Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster : an animal model of disrupted dystrophin-associated glycoprotein complex.
Sakamoto A, Ono K, Abe M, Jasmin G, Eki T, Murakami Y, Masaki T, Toyo-oka T, Hanaoka F.
Proc Natl Acad Sci U S A 94(25):13873-8. 1997
8CMD1L, SGCD
Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex.
Sakamoto A, Ono K, Abe M, Jasmin G, Eki T, Murakami Y, Masaki T, Toyo-oka T, Hanaoka F.
Proc Natl Acad Sci U S A 94(25):13873-8. 1997
9SGCD
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein.
Nigro V, et al.
Hum Mol Genet 5 : 1179-1186. 1996
10SGCD, LGMD2F
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
Nigro V, et al.
Nat Genet 14 : 195-198. 1996
11SGCD, LGMD2F
Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy.
Jung D, et al.
J Biol Chem 271 : 32321-32329. 1996