Author:
Patzkó Ágnes,Shy Michael E.
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Neuroscience
Reference55 articles.
1. Lupski JR, de Oca-Luna RM, Slaugenhaupt S, et al.: DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 1991, 66:219–232.
2. Raeymaekers P, Timmerman V, Nelis E, et al.: Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group. Neuromuscul Disord 1991, 1:93–97.
3. •• Saporta ASD, Sottile S.L., Miller LJ, et al.: Charcot Marie Tooth (CMT) Subtypes and Genetic Testing Strategies Ann Neurol, In Press. This manuscript provides algorithms for genetic testing in CMT based on more than 1000 patients evaluated in a single clinic.
4. Shy ME, Jani A, Krajewski K, et al.: Phenotypic clustering in MPZ mutations. Brain 2004, 127:371–384.
5. Warner LE, Mancias P, Butler IJ, et al.: Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies. Nat Genet 1998, 18:382–384.
Cited by
127 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