Author:
Othmane Kamel Ben,Johnson Ellen,Menold Marisa,Graham Felicia L.,Hamida Mongi Ben,Hasegawa Osamu,Rogala Allison D.,Ohnishi Akio,Pericak-Vance Margaret,Hentati Faycal,Vance Jeffery M.
Reference25 articles.
1. Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding in two siblings;Barbieri;Can. J. Neurol. Sci.,1994
2. Formes pures de la maladie de Charcot–Marie–Tooth (HMSN) en Tunisie. Etude clinique, genealogique, electrophysiologique et histologique de 82 families;Ben Othmane,1990
3. Linkage of a locus (CMT4A) for autosomal recessive Charcot–Marie–Tooth disease to chromosome 8q;Ben Othmane;Hum. Mol. Genet.,1993
4. : Linkage of Charcot–Marie–Tooth neuropathy to the Duffy locus on chromosome 1;Bird;Am. J. Hum. Genet.,1980
5. Localization of a gene responsible for autosomal recessive demyelination neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing;Bolino;Hum. Mol. Genet.,1996
Cited by
62 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献