Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports - United Kingdom
doi 10.1038/srep22913
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Novel GRN Mutation Presenting as an Aphasic Dementia and Evolving Into Corticobasal Syndrome

Neurology: Genetics
NeurologyGenetics
2017English

Novel Mutations in COL4A3, COL4A4, and COL4A5 in Chinese Patients With Alport Syndrome

PLoS ONE
Multidisciplinary
2017English

Numerosity Impairment in Corticobasal Syndrome.

Neuropsychology
Physiological PsychologyNeuropsychology
2010English

Novel IRF6 Mutations in Honduran Van Der Woude Syndrome Patients

Molecular Medicine Reports
OncologyGeneticsMolecular BiologyBiochemistryCancer ResearchMolecular Medicine
2011English

Dopamine Transporter SPECT Imaging in Corticobasal Syndrome

PLoS ONE
Multidisciplinary
2011English

391 Validating Causative Mutations in Patients With Ehlers-Danlos Syndrome Using a Novel Xenograft Model

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2019English

Novel Mutations in BCOR in Three Patients With Oculo-Facio-Cardio-Dental Syndrome, but None in Lenz Microphthalmia Syndrome

European Journal of Human Genetics
Genetics
2005English

Three Novel PAX6 Mutations in Patients With Aniridia

Molecular Pathology
2003English

Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients

PLoS ONE
Multidisciplinary
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy