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1
Q45345293-E44B21D5-E8E9-4E86-B027-6AE942E8945D
Q45345293-E44B21D5-E8E9-4E86-B027-6AE942E8945D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45345293-E44B21D5-E8E9-4E86-B027-6AE942E8945D
Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis.
P2860
Q45345293-E44B21D5-E8E9-4E86-B027-6AE942E8945D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45345293-E44B21D5-E8E9-4E86-B027-6AE942E8945D
rank
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type
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Statement
wasDerivedFrom
d2360ca745640befa0ff96b746ddd325ef553ac5
P2860
The human solute carrier gene SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-N-acetylglucosamine