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| Clinical Characteristics and Neurologic Outcomes of X-Linked Myotubular Myopathy |
| Hyewon Woo, Seungbok Lee, Ji Yeon Han, Woo Joong Kim, Man Jin Kim, Moon-Woo Seong, Soo Yeon Kim, Anna Cho, Byung Chan Lim, Ki Joong Kim, Jong-Hee Chae |
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Ann Child Neurol. 2022;30(3):127-133. Published online June 23, 2022 DOI: https://doi.org/10.26815/acn.2022.00171 |
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Corrigendum: Clinical Characteristics and Neurologic Outcomes of X-Linked Myotubular Myopathy Annals of Child Neurology. 2022;30(4):220-220  Clinical Characteristics and Neurologic Outcomes of X-Linked Myotubular Myopathy Annals of Child Neurology. 2022;30(3):127-133 X-linked myotubular myopathy in a family with three adult survivors Clinical Genetics. 2003;64(2):148-152 X-linked myotubular myopathy: mutation R69C identified in a family with multiple neonatal deaths Clinical Genetics. 2005;67(5):441-442 Underdiagnosis of X-linked myotubular myopathy and other forms of centronuclear myopathy Neuromuscular Disorders. 2007;17(3):266 Germline mosaicism in X-linked myotubular myopathy Clinical Genetics. 1999;56(1):77-81 X-linked myotubular myopathy: clinical and pathological findings in a family Clinical Genetics. 2008;36(1):5-14 International consortium on X-linked myotubular myopathy Brain and Development. 1993;15(4):327 X-linked myotubular myopathy and chylothorax Neuromuscular Disorders. 2008;18(2):183-184 414. A Novel Clinical Severity Scoring Measure in Canine X-Linked Myotubular Myopathy: Results Following Systemic AAV Gene Replacement Molecular Therapy. 2014;22:S158-S159 |
