scholarly article | Q13442814 |
P50 | author | Heather C. Mefford | Q92098631 |
P2860 | cites work | Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation | Q24534159 |
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 development | Q91947691 | ||
Mendelian Gene Discovery: Fast and Furious with No End in Sight | Q93151439 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International | Q24082749 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 2 | |
P921 | main subject | phenotype | Q104053 |
P304 | page(s) | 88-89 | |
P577 | publication date | 2020-02-17 | |
P1433 | published in | Epilepsy Currents | Q5382972 |
P1476 | title | Phenotype to Genotype and Back Again | |
P478 | volume | 20 |
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