Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA study
Spinal muscular atrophy (SMA) is a monogenic disorder caused by loss of function mutations in the survival motor neuron 1 gene, which results in a broad range of disease severity, from neonatal to adult onset. There is currently a concerted effort to define the natural history of the disease and dev...
المؤلفون الرئيسيون: | , , , , , , , , , , , , , , , , , , , , , |
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مؤلفون آخرون: | |
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
Public Library of Science
2018
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