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Q37301164-1A703DBC-8FB8-4E80-A595-E897F7061EA7
Q37301164-1A703DBC-8FB8-4E80-A595-E897F7061EA7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37301164-1A703DBC-8FB8-4E80-A595-E897F7061EA7
RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome
P2860
Q37301164-1A703DBC-8FB8-4E80-A595-E897F7061EA7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37301164-1A703DBC-8FB8-4E80-A595-E897F7061EA7
rank
NormalRank
type
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Statement
wasDerivedFrom
85c3c28d0e62f2fba8a8eb89c0ca6382e8683316
P2860
Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene