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1
s12881-018-0556-2
s12881-018-0556-2
https://scigraph.springernature.com/pub.10.1186/s12881-018-0556-2
Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report.
P2888
Q52664082-1CB8EC26-06F6-4FFF-9300-CF3D74E88111
P2888
s12881-018-0556-2
https://scigraph.springernature.com/pub.10.1186/s12881-018-0556-2