| Geno
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Mag
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Summary
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| (G;G)
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0
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common in complete genomics
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Associated with risk of amyotrophic lateral sclerosis (ALS) in two European populations [PMID 18184915]
[PMID 20711061
] Prion Protein Codon 129 Polymorphism Modifies Age at Onset of Frontotemporal Dementia With the C.709-1G>A Progranulin Mutation
[PMID 18192287] Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.
[PMID 19625741] Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.
[PMID 19640594] Recent insights into the molecular genetics of dementia.
[PMID 21343707] MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?
] Prion Protein Codon 129 Polymorphism Modifies Age at Onset of Frontotemporal Dementia With the C.709-1G>A Progranulin Mutation
