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s12920-018-0362-x
s12920-018-0362-x
https://scigraph.springernature.com/pub.10.1186/s12920-018-0362-x
Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction.
P2888
Q55203941-0983576A-E27B-4832-9D7A-0E0ED9295EA3
P2888
s12920-018-0362-x
https://scigraph.springernature.com/pub.10.1186/s12920-018-0362-x