Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia-Reference-Cited by-同舟云学术

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Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia

Published:1996-04-01 Issue:4 Volume:46 Page:1112-1117
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Cambi F.,Tang X.-M.,Cordray P.,Fain P. R.,Keppen L. D.,Barker D. F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference34 articles.

1. Emery-Dreifuss syndrome and X-linked muscular dystrophy with contractures: evidence for homogeneity

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