Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia-Reference-Cited by-同舟云学术

Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia

Published:1995-08-14 Issue:4 Volume:60 Page:307-311
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Speer Marcy C.,Kingston Helen M.,Boustany Rose-Mary N.,Gaskell Peter C.,Robinson L. Christi,Lennon Felicia,Wolpert Chantelle M.,Yamaoka Larry H.,Kahler Stephen G.,Hogan Edward L.,Cumming W. J. K.,Pericak-Vance Margaret A.

Publisher

Wiley

Subject

Genetics (clinical)

Reference28 articles.

1. Disordered pigmentation, spastic paraparesis and peripheral neuropathy in three siblings: a new neurocutaneous syndrome.

2. ‘Pure’ and ‘Complicated’ Forms of Hereditary Spastic Paraplegia Presenting in Childhood

3. Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

4. The autosomal dominant form of "pure" familial spastic paraplegia: Clinical findings and linkage analysis of a large pedigree

5. Autosomal dominant familial spastic paraplegia: report of a large New England family

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1. Hereditary Spastic Paraplegia;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

2. Hereditäre spastische Paraplegie mit Beginn im Kindesalter;Monatsschrift Kinderheilkunde;1998-06-24

3. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia;neurogenetics;1997-11-01