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Q27304405-17EA4019-9C91-468F-BBEE-F7B7DD55416A
Q27304405-17EA4019-9C91-468F-BBEE-F7B7DD55416A
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http://www.wikidata.org/entity/statement/Q27304405-17EA4019-9C91-468F-BBEE-F7B7DD55416A
De novo identification of replication-timing domains in the human genome by deep learning
P2860
Q27304405-17EA4019-9C91-468F-BBEE-F7B7DD55416A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27304405-17EA4019-9C91-468F-BBEE-F7B7DD55416A
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wasDerivedFrom
7dd5a13f6cdc8436023d20f582a51911563c4604
P2860
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.