Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.

Author:

De Jonghe P,Timmerman V,FitzPatrick D,Spoelders P,Martin J J,Van Broeckhoven C

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference15 articles.

1. Hereditary motor and sensory neuropathies;Dyck, P.J.; Chance, P.; Lebo, R.; Carney, J.A.,1993

2. The clinical features of hereditary motor and sensory neuropathy types I and II;Harding, A.E.; Thomas, P.K.;Brain,1980

3. Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families;Nicholson, G.; Nash, J.;Neurology,1993

4. Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes lp35-p36 and Xql3;Timmerman, V.; De Jonghe, P.; Spoelders, P.;Neurology,1996

5. A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26;Priest, J.M.; Fischbeck, K.H.; Nouri, N.; Keats, B.J.B.;Genomics,1995

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