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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

Molecular Biology

English

Clinical and Genetic Heterogeneity in Laminopathies

Biochemical Society Transactions

English

Mechanosensing Defects in Nuclear Envelope Related Disorders

Biophysical Journal

English

A New Case of SMA Phenotype Without Epilepsy Due to Biallelic Variants in ASAH1

European Journal of Human Genetics

English

199th ENMC International Workshop: FHL1 Related Myopathies, June 7–9, 2013, Naarden, the Netherlands

Neuromuscular Disorders

English

The 2017 Version of the Gene Table of Monogenic Neuromuscular Disorders (Nuclear Genome)

Neuromuscular Disorders

English

Consequences of Lmna Exon 4 Mutations in Myoblast Function

English

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

American Journal of Human Genetics

English

Proteasome-Mediated Degradation of Integral Inner Nuclear Membrane Protein Emerin in Fibroblasts Lacking A-Type Lamins

Biochemical and Biophysical Research Communications

Molecular Biology

English