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Q41694710-F753D83A-EC69-4D72-B5A4-B7F30302496D
Q41694710-F753D83A-EC69-4D72-B5A4-B7F30302496D
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Statement
http://www.wikidata.org/entity/statement/Q41694710-F753D83A-EC69-4D72-B5A4-B7F30302496D
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder.
P2860
Q41694710-F753D83A-EC69-4D72-B5A4-B7F30302496D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41694710-F753D83A-EC69-4D72-B5A4-B7F30302496D
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wasDerivedFrom
119fecf5945400186e5511b790902460bae488cc
P2860
Generating linkage mapping files from Affymetrix SNP chip data.