Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

Author:

Raeymaekers P,Timmerman V,Nelis E,De Jonghe P,Hoogenduk J.E,Baas F,Barker D.F,Martin J.J,De Visser M,Bolhuis P.A,Van Broeckhoven C

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference17 articles.

1. Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory, and autonomic neurons;Dyck,1984

2. The nosology of genetic peripheral neuropathies in Swedish children;Hagberg;Acta Paediatr Scand,1983

3. Prevalence of hereditary motor and sensory neuropathy in Cantabria;Combarros;Acta Neurol Scand,1987

4. Genetic aspects of hereditary motor and sensory neuropathy (type I and II);Harding;J Med Genet,1980

5. Linkage of dominantly inherited Charcot-Marie-Tooth neuropathy to the Duffy locus in an Indiana family;Stebbins;Am J Hum Genet,1982

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