Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy

Haber G, Conway KM, Paramsothy P, et al. Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy. Muscle & nerve 2020   Abstract BACKGROUND: Quantifying associations between genetic mutations and loss of ambulation (LoA) among males diagnosed with childhood-onset dystrophinopathy is important for understanding variation in disease progression and may be useful in […]