Jocelyn Laporte's team received support from the Rare Diseases Foundation for a high-throughput sequencing project. This study led to the discovery of a new gene involved in centronuclear myopathies in a French family.
Jocelyn Laporte's team received support from the Rare Diseases Foundation for a high-throughput sequencing project. This study led to the discovery of a new gene involved in centronuclear myopathies in a French family.