Ewa Chelmicka-Schorr to Humans
This is a "connection" page, showing publications Ewa Chelmicka-Schorr has written about Humans.
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A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex. Neuromuscul Disord. 2007 Apr; 17(4):285-9.
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A variant of Fukuyama congenital muscular dystrophy in a non-Japanese child. Pediatr Neurol. 1986 Sep-Oct; 2(5):290-3.
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