Phenotype to Genotype and Back Again

scientific article published on 17 February 2020

Phenotype to Genotype and Back Again is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1177/1535759720901734
P932PMC publication ID7160881
P698PubMed publication ID32313504

P50authorHeather C. MeffordQ92098631
P2860cites workMutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardationQ24534159
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.Q33910551
CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and developmentQ91947691
Mendelian Gene Discovery: Fast and Furious with No End in SightQ93151439
P275copyright licenseCreative Commons Attribution-NonCommercial-NoDerivs 4.0 InternationalQ24082749
P6216copyright statuscopyrightedQ50423863
P433issue2
P921main subjectphenotypeQ104053
P304page(s)88-89
P577publication date2020-02-17
P1433published inEpilepsy CurrentsQ5382972
P1476titlePhenotype to Genotype and Back Again
P478volume20

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