84 citations
- Centre Hospitalier Universitaire de LilleFR7 papers
- InsermFR7 papers
- Université de LilleFR6 papers
- Assistance Publique – Hôpitaux de ParisFR3 papers
- Centre National de la Recherche ScientifiqueFR3 papers
- Institut de Biologie de LilleFR3 papers
- Pitié-Salpêtrière HospitalFR3 papers
- Sorbonne UniversitéFR3 papers
- Institut de Psychiatrie et Neurosciences de ParisFR2 papers
- Institut du CerveauFR2 papers
- Lille Neurosciences & Cognition2 papers
- Centre Oscar LambretFR1 paper
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q-bio.GN2021
Reply: Early-onset phenotype of bi-allelic GRN mutations
Vincent Huin, Mathieu Barbier, Alexandra Durr +1
We would like to reply to Neuray et al. who report a series of five new patients from four unrelated families with bi-allelic mutations of GRN. Their work nicely completes the few…
q-bio.GN2020★ 27 cited
Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsy
Vincent Huin, Isabelle Strubi-Vuillaume, Kathy Dujardin +10
BACKGROUND: Spinocerebellar ataxia types 19 and 22 (SCA19/22) are rare conditions in which relatively isolated cerebellar involvement is frequently associated with cognitive impair…
q-bio.GN2020★ 35 cited
The MAPT gene is differentially methylated in the progressive supranuclear palsy brain
Vincent Huin, Vincent Deramecourt, Dominique Caparros-Lefebvre +10
Background: Progressive supranuclear palsy (PSP) is a rare neurodegenerative disease causing parkinsonian symptoms. Altered DNA methylation of the microtubule-associated protein ta…