Author:
Cao Henian,Hegele Robert A.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference23 articles.
1. Arboleda H, Quintero L, Yunis E (1997) Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients. J Med Genet 34:433–437
2. Bitoun P, Lachassine E, Sellier N, Sauvion S, Gaudelus J (1995) The Wiedemann-Rautenstrauch neonatal progeroid syndrome: a case report and review of the literature. Clin Dysmorph 4:239–245
3. Bonne G, Raffaele di Barletta M, Varnous S, Becane HM, Hammouda EH, Merlini L, Muntoni F, Greenberg CR, Gary F, Urtizberea JA, Duboc D, Fardeau M, Toniolo D, Schwartz K (1999) Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet 21:285–288
4. Brown WT, Abdenur J, Goonewardena P, Alemzadeh R, Smith M, Friedman S, Cervantes C, Bandyopadhyay S, Zaslav A, Kunaporn S, Serotkin A, Lifshitz F (1990) Hutchinson-Gilford progeria syndrome: clinical, chromosomal and metabolic abnormalities (Abstract). Am J Hum Genet 47:A50
5. Burke B, Stewart CL (2002) Life at the edge: the nuclear envelope and human disease. Nat Rev Mol Cell Biol 3:575–585
Cited by
192 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献