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2. Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin. Tachi N; Ohya K; Chiba S; Matsuo M; Patria SY; Matsumura K Neurology; 1997 Aug; 49(2):579-83. PubMed ID: 9270600 [TBL] [Abstract][Full Text] [Related]
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19. Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging. Philpot J; Cowan F; Pennock J; Sewry C; Dubowitz V; Bydder G; Muntoni F Neuromuscul Disord; 1999 Mar; 9(2):81-5. PubMed ID: 10220862 [TBL] [Abstract][Full Text] [Related]
20. Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity? Mercuri E; Sewry CA; Brown SC; Brockington M; Jungbluth H; DeVile C; Counsell S; Manzur A; Muntoni F Neuropediatrics; 2000 Aug; 31(4):186-9. PubMed ID: 11071142 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]