Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/11468
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Type: Journal article
Title: A novel mutation in Exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegia
Author: Donnelly, A.
Colley, A.
Crimmins, D.
Mulley, J.
Citation: Human Mutation, 1996; 8(4):384-385
Publisher: Hindawi Limited
Issue Date: 1996
ISSN: 1059-7794
1098-1004
Statement of
Responsibility: 
Donnelly, Andrew ; Colley, Alison ; Crimmins, Denis ; Mulley, John
Keywords: X Chromosome
Humans
Paraplegia
Myelin Proteolipid Protein
Genetic Markers
Chromosome Mapping
Restriction Mapping
Lod Score
Point Mutation
Exons
Child
Female
Male
Genetic Linkage
Genetic Carrier Screening
DOI: 10.1002/(SICI)1098-1004(1996)8:4<384::AID-HUMU17>3.0.CO;2-Z
Published version: http://dx.doi.org/10.1002/(sici)1098-1004(1996)8:4%3C384::aid-humu17%3E3.0.co;2-z
Appears in Collections:Aurora harvest 7
Genetics publications

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