Author:
Kakavand B.,Schroeder V.A.,Di Sessa T. G.
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology, and Child Health
Reference7 articles.
1. Bhan AK, Brody C (2001) Propionic acidemia: a rare cause of Cardiomyopathy. Congestive Heart Failure 7:218–219
2. Jiang C, Atkinson DL, Towbin JA, Splawski I, et al. (1994) Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity. Na Genet 8:141–147
3. Keating MT, Dunn C, Atkinson DL, et al. (1991) Consistent linkage of the long QT syndrome to the Harvey ras-1 locus on chromosome 11. Ann J Hum Genet 49:1335–1339
4. Perez-Cerda C, Clavero S, Perez B, et al. (2003) Functional analysis of PCCB mutations causing propionic acidemia based on expression studies in deficient human skin fibroblasts. Biochim Biophys Acta 1638:43–49
5. Shimizu W, Noda T, Takaki H, et al. (2003) Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome. J Am Coll Cardiol 41:633–642
Cited by
28 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