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Q58611455-2AD46603-3467-48D6-B0EE-88C576D03A41
Q58611455-2AD46603-3467-48D6-B0EE-88C576D03A41
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58611455-2AD46603-3467-48D6-B0EE-88C576D03A41
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
P2860
Q58611455-2AD46603-3467-48D6-B0EE-88C576D03A41
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58611455-2AD46603-3467-48D6-B0EE-88C576D03A41
rank
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type
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Statement
wasDerivedFrom
ef92bcb8cc81c4d4a95aca1c1a8e4f71d85f1dc0
P2860
Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing Loss