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Q48437995-B64004B1-0DDC-4DF3-9A74-71AFD66CAD19
Q48437995-B64004B1-0DDC-4DF3-9A74-71AFD66CAD19
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Statement
http://www.wikidata.org/entity/statement/Q48437995-B64004B1-0DDC-4DF3-9A74-71AFD66CAD19
MED20 mutation associated with infantile basal ganglia degeneration and brain atrophy.
P2860
Q48437995-B64004B1-0DDC-4DF3-9A74-71AFD66CAD19
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48437995-B64004B1-0DDC-4DF3-9A74-71AFD66CAD19
rank
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wasDerivedFrom
404a06d9e95418feda0a5bb6128d626f70e9e48e
P2860
Mutations in MED12 cause X-linked Ohdo syndrome