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Q39448846-21F209F3-D10A-4CCB-A915-11C74E0EDAFC
Q39448846-21F209F3-D10A-4CCB-A915-11C74E0EDAFC
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Statement
http://www.wikidata.org/entity/statement/Q39448846-21F209F3-D10A-4CCB-A915-11C74E0EDAFC
Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders.
P2860
Q39448846-21F209F3-D10A-4CCB-A915-11C74E0EDAFC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39448846-21F209F3-D10A-4CCB-A915-11C74E0EDAFC
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Statement
wasDerivedFrom
9fcc2c19a7eff0377d0ac8aec71afc8eed2dee1c
P2860
Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families.