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| Congenital muscular dystrophy type 1A with residual merosin expression |
| Hyo Jeong Kim, Young-Chul Choi, Hyung Jun Park, Young-Mock Lee, Heung Dong Kim, Joon Soo Lee, Hoon-Chul Kang |
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Clin Exp Pediatr. 2014;57(3):149-152. Published online March 31, 2014 DOI: https://doi.org/10.3345/kjp.2014.57.3.149 |
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Congenital muscular dystrophy type 1A with residual merosin expression Korean Journal of Pediatrics. 2014;57(3):149  Congenital Muscular Dystrophy Type 1A Genetic Neuromuscular Disorders. 2017;99-103 Occidental-type cerebromuscular dystrophy versus congenital muscular dystrophy with merosin deficiency Child's Nervous System. 1998;14(10):531-531 Brain MRI features of merosin-negative congenital muscular dystrophy Australasian Radiology. 2007;51:B221-B223 Electrophysiological and pathological studies of peripheral nerves in children with merosin-deficient congenital muscular dystrophy type 1A Neuromuscular Disorders. 2017;27:S108 P289 – 2042 Merosin-deficient congenital muscular dystrophy type 1A (MDC1A): a case report European Journal of Paediatric Neurology. 2013;17:S133 Congenital Muscular Dystrophy Type 1A Genetic Neuromuscular Disorders. 2014;83-87 Severe classical congenital muscular dystrophy and merosin expression Clinical Genetics. 2008;54(3):193-198 Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal Neuromuscular Disorders. 1995;5(4):301-305 Limitation of eye movement in merosin-deficient congenital muscular dystrophy The Lancet. 1999;353(9149):297-298 |
