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Q34479643-9D9D0FD1-E3C7-487E-BBC8-4C3846BCE1AB
Q34479643-9D9D0FD1-E3C7-487E-BBC8-4C3846BCE1AB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34479643-9D9D0FD1-E3C7-487E-BBC8-4C3846BCE1AB
Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasias.
P2860
Q34479643-9D9D0FD1-E3C7-487E-BBC8-4C3846BCE1AB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34479643-9D9D0FD1-E3C7-487E-BBC8-4C3846BCE1AB
rank
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wasDerivedFrom
b124bedd475b31c4f48286af971253095464ac5b
P2860
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.