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Q50092105-E8FB2A5B-45D6-4B93-9B97-E903500F4D7E
Q50092105-E8FB2A5B-45D6-4B93-9B97-E903500F4D7E
BestRank
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http://www.wikidata.org/entity/statement/Q50092105-E8FB2A5B-45D6-4B93-9B97-E903500F4D7E
Mild Zellweger syndrome due to a novel PEX6 mutation: correlation between clinical phenotype and in silico prediction of variant pathogenicity.
P2860
Q50092105-E8FB2A5B-45D6-4B93-9B97-E903500F4D7E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50092105-E8FB2A5B-45D6-4B93-9B97-E903500F4D7E
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wasDerivedFrom
bd3a27aebc055dd290b74da65b48bfa8168f3d2b
P2860
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.