Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1

44Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.

Abstract

Data from English families confirms the probable linkage of the loci for autosomal dominant type I hereditary motor and sensory neuropathy (HMSN) and the Duffy blood group. The locus for autosomal dominant type I HMSN is in chromosome 1 near the centromere, about 15 centimorgans from the Duffy locus. The linkage between type I HMSN and the Duffy locus and the two recombinants found between Duffy and type II HMSN support the hypothesis that there are at least two genetic variants of autosomal dominant HMSN.

Cite

CITATION STYLE

APA

Guiloff, R. J., Thomas, P. K., Contreras, M., Armitage, S., Schwarz, G., & Sedgwick, E. M. (1982). Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1. Journal of Neurology Neurosurgery and Psychiatry, 45(8), 669–674. https://doi.org/10.1136/jnnp.45.8.669

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free