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Q56866613-5CB1AC92-9107-4822-BFC9-8CACC3B0BDA4
Q56866613-5CB1AC92-9107-4822-BFC9-8CACC3B0BDA4
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http://www.wikidata.org/entity/statement/Q56866613-5CB1AC92-9107-4822-BFC9-8CACC3B0BDA4
A Point Mutation at the X-Chromosomal Proteolipid Protein Locus in Pelizaeus-Merzbacher Disease Leads to Disruption of Myelinogenesis
P2860
Q56866613-5CB1AC92-9107-4822-BFC9-8CACC3B0BDA4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q56866613-5CB1AC92-9107-4822-BFC9-8CACC3B0BDA4
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type
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wasDerivedFrom
50f626d35abf7e01dde340b7aca37a4465dd2837
P2860
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant