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UnknownScreening for C9ORF72 repeat expansion in FTLD.
Not available
S-EPMC3743244 | biostudies-literature
UnknownThe broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene.
Not available
S-EPMC9153267 | biostudies-literature
UnknownPSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response.
Not available
S-EPMC11267520 | biostudies-literature
UnknownEffects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
Not available
S-EPMC4314944 | biostudies-literature
UnknownOne Health Investigation of SARS-CoV-2 Infection and Seropositivity among Pets in Households with Confirmed Human COVID-19 Cases-Utah and Wisconsin, 2020.
Not available
S-EPMC8472995 | biostudies-literature
UnknownExpanding the phenotypic spectrum of ARCN1-related syndrome.
Not available
S-EPMC9923403 | biostudies-literature
UnknownGlobal and local ancestry in African-Americans: Implications for Alzheimer's disease risk.
Not available
S-EPMC4681680 | biostudies-literature
UnknownGenetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
Not available
S-EPMC3160280 | biostudies-literature
UnknownHeterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Not available
S-EPMC11739880 | biostudies-literature
UnknownDe Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay.
Not available
S-EPMC7332645 | biostudies-literature
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