Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Gisèle Bonne
DelK32-lamin a/C Has Abnormal Location and Induces Incomplete Tissue Maturation and Severe Metabolic Defects Leading to Premature Death
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
Clinical and Genetic Heterogeneity in Laminopathies
Biochemical Society Transactions
Biochemistry
Mechanosensing Defects in Nuclear Envelope Related Disorders
Biophysical Journal
Biophysics
A New Case of SMA Phenotype Without Epilepsy Due to Biallelic Variants in ASAH1
European Journal of Human Genetics
Genetics
199th ENMC International Workshop: FHL1 Related Myopathies, June 7–9, 2013, Naarden, the Netherlands
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
The 2017 Version of the Gene Table of Monogenic Neuromuscular Disorders (Nuclear Genome)
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Consequences of Lmna Exon 4 Mutations in Myoblast Function
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
American Journal of Human Genetics
Genetics
Proteasome-Mediated Degradation of Integral Inner Nuclear Membrane Protein Emerin in Fibroblasts Lacking A-Type Lamins
Biochemical and Biophysical Research Communications
Biochemistry
Cell Biology
Molecular Biology
Biophysics