X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus (Q55670712)

2

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D Bonneau

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J M Rozet

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M Le Merrer

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R Gil

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O Boespflug-Tanguy

https://scigraph.springernature.com/pub.10.1038/ng0394-257

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language of work or name

English

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publication date

March 1994

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published in

Nature Genetics

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volume

6

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issue

3

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page(s)

257-62

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exact match

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cites work

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Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder

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Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant

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A new mutation in the proteolipid protein (PLP) gene in a German family with pelizaeus-merzbacher disease

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Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders

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