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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Disease and SLC25A27[original query]
Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG.
Neuroscience letters 2006 Mar 396 (2): 137-42.
Norberg Anna, Forsgren Lars, Holmberg Dan, Holmberg Moni
Uncoupling protein 4 (UCP4) gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementia.
Aging 2018 11 10 (11): 3283-3293.
Montesanto Alberto, Crocco Paolina, Dato Serena, Geracitano Silvana, Frangipane Francesca, Colao Rosanna, Maletta Raffaele, Passarino Giuseppe, Bruni Amalia C, Rose Giuseppi
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