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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
Lee, S.J. van der; Conway, O.J.; Jansen, I.; Carrasquillo, M.M.; Kleineidam, L.; Akker, E. van den; ... ; GIFT Genetic Invest 2019
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
Article / Letter to editor
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Homozygous and Compound-Heterozygous Mutations in TGDS Cause Catel-Manzke Syndrome
Ehmke, N.; Caliebe, A.; Koenig, R.; Kant, S.G.; Stark, Z.; Cormier-Daire, V.; ... ; Mundlos, S. 2014
Homozygous and Compound-Heterozygous Mutations in TGDS Cause Catel-Manzke Syndrome
Article / Letter to editor
metadata only