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Q34141813-6960D373-9AB0-410F-B9C8-1108C3E14A50
Q34141813-6960D373-9AB0-410F-B9C8-1108C3E14A50
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Statement
http://www.wikidata.org/entity/statement/Q34141813-6960D373-9AB0-410F-B9C8-1108C3E14A50
Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosome.
P2860
Q34141813-6960D373-9AB0-410F-B9C8-1108C3E14A50
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34141813-6960D373-9AB0-410F-B9C8-1108C3E14A50
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wasDerivedFrom
a4803ca5e4fd8f2d0d63181b9d6c65837619a9d8
P2860
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome