Literature DB >> 8492918

Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a).

J E Hoogendijk1, E A Janssen, A A Gabreëls-Festen, G W Hensels, E M Joosten, F J Gabreëls, I Zorn, L J Valentijn, F Baas, B W Ongerboer de Visser.   

Abstract

The most frequently found mutation in autosomal dominant hereditary motor and sensory neuropathy type I (HMSN I) is a large duplication on chromosome 17p11.2 containing probes VAW409R3, VAW412R3, and EW401. We investigated a family with severe features of HMSN I, and demonstrated the absence of this duplication by a quantitative analysis of the hybridization signals of VAW409R3 and VAW412R3. Linkage analysis, however, revealed linkage with probe VAW409R3a (lod score, 3.22), which demonstrates the existence of allelic heterogeneity within the HMSN Ia locus. These findings have implications for clinical practice and for investigating the identity of the HMSN Ia gene.

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Year:  1993        PMID: 8492918     DOI: 10.1212/wnl.43.5.1010

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  4 in total

1.  Effectiveness of real-time quantitative PCR compare to repeat PCR for the diagnosis of Charcot-Marie-Tooth Type 1A and hereditary neuropathy with liability to pressure palsies.

Authors:  Jong Rak Choi; Woon Hyoung Lee; Il Nam Sunwoo; Eun Kyung Lee; Chang Hoon Lee; Jong Baeck Lim
Journal:  Yonsei Med J       Date:  2005-06-30       Impact factor: 2.759

Review 2.  Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.

Authors:  Anneke Gabreëls-Festen
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

3.  Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutations.

Authors:  A A Gabreëls-Festen; P A Bolhuis; J E Hoogendijk; L J Valentijn; E J Eshuis; F J Gabreëls
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

4.  PMP22 exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E.

Authors:  David S Wang; Xingyao Wu; Yunhong Bai; Craig Zaidman; Tiffany Grider; John Kamholz; James R Lupski; Anne M Connolly; Michael E Shy
Journal:  Ann Clin Transl Neurol       Date:  2017-03-12       Impact factor: 4.511

  4 in total

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