Wikidata

(Q52533780)

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

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title
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)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9934976
retrieved
2 May 2018
reference URL
http://europepmc.org/abstract/MED/9934976
author name string
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