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Q54319740-3EB7ADC0-12FE-48B4-845A-CEAFB09690BB
Q54319740-3EB7ADC0-12FE-48B4-845A-CEAFB09690BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54319740-3EB7ADC0-12FE-48B4-845A-CEAFB09690BB
A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain.
P2860
Q54319740-3EB7ADC0-12FE-48B4-845A-CEAFB09690BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54319740-3EB7ADC0-12FE-48B4-845A-CEAFB09690BB
rank
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type
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Statement
wasDerivedFrom
d95f8f4fae98856fa434e97ddf04a07a6a91cb75
P2860
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum