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Publications by François Rivier
A Missense Mutation Within the Fork-Head Domain of the Forkhead Box G1 Gene (FOXG1) Affects Its Nuclear Localization
Human Mutation
Genetics
The 2017 Version of the Gene Table of Monogenic Neuromuscular Disorders (Nuclear Genome)
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Related publications
Author Correction: Characterization of a Recurrent Missense Mutation in the Forkhead DNA-binding Domain of FOXP1
Scientific Reports
Multidisciplinary
The Clinicopathological Significance of Forkhead Box P1 and Forkhead Box O3a in Pancreatic Ductal Adenocarcinomas
Tumor Biology
Medicine
Cancer Research
FOXC1 (Forkhead Box C1)
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
Identification of a Novel Missense Mutation in NIPAL4 Gene: First 3D Model Construction Predicted Its Pathogenicity
Molecular genetics & genomic medicine
Genetics
Molecular Biology
A De Novo Missense Mutation in a Critical Domain of the X-Linked DDP Gene Causes the Typical Deafness–dystonia–optic Atrophy Syndrome
European Journal of Human Genetics
Genetics
Identification of Missense Mutation (I12T) in the BSND Gene and Bioinformatics Analysis
Journal of Biomedicine and Biotechnology
A Novel Missense Mutation of F 9 Gene in Hemophilia B Patients
Journal of Blood Disorders & Transfusion
A Novel Missense Mutation T101N in the Melanocortin-4 Receptor Gene Associated With Obesity
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
The Novel Missense Mutation Met48Lys in FKBP22 Changes Its Structure and Functions
Scientific Reports
Multidisciplinary
