Libyan Families Demand Probe Into Delayed SMA Gene Therapy for Children
Patients with spinal muscular atrophy (SMA) and their families have issued a strongly worded statement holding the Support and Development ...
Read morePatients with spinal muscular atrophy (SMA) and their families have issued a strongly worded statement holding the Support and Development ...
Read moreThe head of Libya’s Muscular Dystrophy Patients Association, Mohamed Abu Ghmeyqa, has raised alarm over the deteriorating health condition of ...
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