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Q55058977-009C084E-B556-4F4A-8D52-9879EDD41125
Q55058977-009C084E-B556-4F4A-8D52-9879EDD41125
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http://www.wikidata.org/entity/statement/Q55058977-009C084E-B556-4F4A-8D52-9879EDD41125
Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene.
P2860
Q55058977-009C084E-B556-4F4A-8D52-9879EDD41125
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55058977-009C084E-B556-4F4A-8D52-9879EDD41125
rank
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type
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wasDerivedFrom
9e2b742cad9095ffe28e05691713593fa0d9840f
P2860
Mutation type and position varies between mosaic and inherited NF2 and correlates with disease severity