Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
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Reply: PRUNE1: a disease-causing gene for secondary microcephaly.PRUNE1: a disease-causing gene for secondary microcephaly.Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing.PRUNE Syndrome Is a New Neurodevelopmental Disorder: Report and Review.
P2860
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
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Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
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Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
@nl
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Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
@en
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
@nl
prefLabel
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
@en
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
@nl
P2093
P2860
P356
P1476
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype
@en
P2093
Gregory Costain
Peter Kannu
Pradeep Krishnan
Saadet Mahmutoglu
Suzanne Laughlin
P2860
P304
P356
10.1002/AJMG.A.38066
P407
P577
2017-03-01T00:00:00Z