| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 18832141 [Unique ID], provided by the PubMed system | |
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| | 1 - 10 of 102 journal articles in the PubMed database | Email to a friend | | |
| Houlden H, Laura M, Wavrant-De Vrièze F, et al.
Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2. [JOURNAL ARTICLE]
Neurology 2008 Oct 1.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Rohkamm B, Reilly MM, Lochmüller H, et al.
Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome. [JOURNAL ARTICLE]
J Neurol Sci 2007 Jul 27.
Abstract | Full Citation | | Takashima H
[Molecular genetics of inherited neuropathies] [Journal Article, Review]
Rinsho Shinkeigaku 2006 Jan; 46(1):1-18.
Abstract | Full Citation | Find Related Articles | | Evgrafov OV, Mersiyanova I, Irobi J, et al.
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. [Journal Article]
Nat Genet 2004 Jun; 36(6):602-6.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Tang B, Liu X, Zhao G, et al.
Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease. [Journal Article]
Arch Neurol 2005 Aug; 62(8):1201-7.
Abstract | Full Citation | | Chung KW, Kim SB, Cho SY, et al.
Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation. [Journal Article]
Exp Mol Med 2008 Jun 30; 40(3):304-12.
Abstract | Full Citation | | Dierick I, Baets J, Irobi J, et al.
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study. [JOURNAL ARTICLE]
Brain 2008 Mar 5.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Tang BS, Zhao GH, Luo W, et al.
Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L. [Journal Article]
Hum Genet 2005 Feb; 116(3):222-4.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | De Sandre-Giovannoli A, Chaouch M, Kozlov S, et al.
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse. [Journal Article]
Am J Hum Genet 2002 Mar; 70(3):726-36.
Abstract | Full Citation |   |
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