Literature DB >> 2725880

Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markers.

P Raeymaekers1, P De Jonghe, H Backhovens, A Wehnert, G De Winter, L Swerts, J Gheuens, J J Martin, A Vandenberghe, C Van Broeckhoven.   

Abstract

We previously reported a large Charcot-Marie-Tooth family not linked to the Duffy blood group marker, supporting the existence of genetic heterogeneity in this neuropathy. In order to investigate the possibility of another disease locus on chromosome 1, we analyzed this family further, using DNA polymorphisms of 6 genes. Absence of linkage makes a second disease locus on chromosome 1 unlikely.

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Year:  1989        PMID： 2725880     DOI： 10.1212/wnl.39.6.844

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


  3 in total

1.  Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

Authors:  P Raeymaekers; V Timmerman; P De Jonghe; L Swerts; J Gheuens; J J Martin; L Muylle; G De Winter; A Vandenberghe; C Van Broeckhoven
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

2.  Hereditary motor and sensory neuropathy type I and type II.

Authors:  A Sghirlanzoni; D Pareyson; V Scaioli; R Marazzi; L Pacini
Journal:  Ital J Neurol Sci       Date:  1990-10

Review 3.  A molecular basis for hereditary motor and sensory neuropathy disorders.

Authors:  M E Shy; J Balsamo; J Lilien; J Kamholz
Journal:  Curr Neurol Neurosci Rep       Date:  2001-01       Impact factor: 5.081
  3 in total

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