X-linked recessive myotubular myopathy with mutations

X-linked recessive myotubular myopathy (XLMTM) is a severe congenital muscle disorder caused by mutations in the MTM1 gene and characterized by severe hypotonia and generalized muscle weakness in affected males. It is generally a fatal disorder during the neonatal period and early infancy. The diagn...

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Main Authors: Young-Mi Han (Author), Kyoung-Ah Kwon (Author), Yun-Jin Lee (Author), Sang-Ook Nam (Author), Kyung-Hee Park (Author), Shin-Yun Byun (Author), Gu-Hwan Kim (Author), Han-Wook Yoo (Author)
Format: Book
Published: Korean Pediatric Society, 2013-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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