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Q50432380-9D2A188B-E289-4309-B8E5-D9F73E2BA1AD
Q50432380-9D2A188B-E289-4309-B8E5-D9F73E2BA1AD
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Statement
http://www.wikidata.org/entity/statement/Q50432380-9D2A188B-E289-4309-B8E5-D9F73E2BA1AD
The ESF meeting on "The proteomics, epigenetics and pharmacogenetics of pendrin".
P2860
Q50432380-9D2A188B-E289-4309-B8E5-D9F73E2BA1AD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50432380-9D2A188B-E289-4309-B8E5-D9F73E2BA1AD
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wasDerivedFrom
f28b619a1d8160484e92a015912595497425abcc
P2860
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)