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Q24337891-936BD6F0-46FB-480F-A2C3-CD5518CA6BDF
Q24337891-936BD6F0-46FB-480F-A2C3-CD5518CA6BDF
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http://www.wikidata.org/entity/statement/Q24337891-936BD6F0-46FB-480F-A2C3-CD5518CA6BDF
Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects
P921
Q24337891-936BD6F0-46FB-480F-A2C3-CD5518CA6BDF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24337891-936BD6F0-46FB-480F-A2C3-CD5518CA6BDF
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type
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wasDerivedFrom
17da9be1f8890cd10616e848aec6b571eb80d078
P921
Xylosyltransferase 2