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| Early-onset Dementia v1.54 | PRKCH | Zornitza Stark Marked gene: PRKCH as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Early-onset Dementia v1.54 | PRKCH | Zornitza Stark Gene: prkch has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Early-onset Dementia v1.54 | PRKCH |
Zornitza Stark gene: PRKCH was added gene: PRKCH was added to Early-onset Dementia. Sources: Literature Mode of inheritance for gene: PRKCH was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PRKCH were set to 40591711 Phenotypes for gene: PRKCH were set to Alzheimer disease, MONDO:0004975, PRKCH-related Review for gene: PRKCH was set to RED Added comment: PMID 40591711 reports eight individuals from one family with a homozygous missense K65R variant Sources: Literature |
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