ArticleAmerican journal of human genetics2001
Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1.
Article in American journal of human genetics, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.
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Who cites it
15 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.
- Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.Journal of neurology · 2017Pooled it
- Understanding the Hidden Complexity of Latin American Population Isolates.American journal of human genetics · 2018Article
- Intermediate Charcot-Marie-Tooth disease.Neuroscience bulletin · 2014Review
- Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth disease.American journal of human genetics · 2013Article
- Molecular genetics of charcot-marie-tooth disease: from genes to genomes.Molecular syndromology · 2012Article
- Shades of gray: a comparison of linkage disequilibrium between Hutterites and Europeans.Genetic epidemiology · 2010Article
- Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.Brain : a journal of neurology · 2009Article
- Dynamic instability of microtubules requires dynamin 2 and is impaired in a Charcot-Marie-Tooth mutant.The Journal of cell biology · 2009Article
- Intermediate forms of Charcot-Marie-Tooth neuropathy: a review.Neuromolecular medicine · 2006Review
- Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.Neuromolecular medicine · 2006Review
- Molecular diagnostics of Charcot-Marie-Tooth disease and related peripheral neuropathies.Neuromolecular medicine · 2006Review
- Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35.American journal of human genetics · 2003Article
- Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region.Neurogenetics · 2003Article
- Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AI1 viral integration site to 14q13.3-q21.1.BMC genomics · 2003Article
- The genetic convergence of Charcot-Marie-Tooth disease types 1 and 2 and the role of genetics in sporadic neuropathy.Current neurology and neuroscience reports · 2002Review
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Authors and funding
6 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Intermediate Charcot-Marie-Tooth neuropathy (CMT) is an inherited sensory motor neuropathy characterized by motor median nerve conduction velocities of 25-45 m/s. We performed a genomewide search in an Italian family with autosomal dominant intermediate CMT and mapped the locus on chromosome 10q. Analysis of key recombinants maps the gene for autosomal dominant intermediate CMT to a 10.7-Mb interval on chromosome 10q24.1-q25.1, between simple tandem repeat markers D10S1709 and D10S1795.
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