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Q41834429-11AC2DAE-49E2-41D4-8BE8-11263963C527
Q41834429-11AC2DAE-49E2-41D4-8BE8-11263963C527
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http://www.wikidata.org/entity/statement/Q41834429-11AC2DAE-49E2-41D4-8BE8-11263963C527
Different subcellular localisations of TRIM22 suggest species-specific function.
P2860
Q41834429-11AC2DAE-49E2-41D4-8BE8-11263963C527
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41834429-11AC2DAE-49E2-41D4-8BE8-11263963C527
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wasDerivedFrom
7b3a381d98ff644654275b5e6165433e0c59fb09
P2860
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome