Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). (Q52533780)
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scientific article published in January 1999
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). |
scientific article published in January 1999 |
Statements
Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). (English)
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Hodes ME
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Zimmerman AW
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Aydanian A
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Naidu S
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Miller NR
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Garcia Oller JL
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Barker B
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Aleck KA
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Hurley TD
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Dlouhy SR
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1 January 1999
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82
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2
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132-139
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