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DDY277
DDY277
http://dx.doi.org/10.1093/HMG/DDY277
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P356
Q57484322-FDB9AA4C-F24A-489C-864A-5AD200F38A14
P356
DDY277
http://dx.doi.org/10.1093/HMG/DDY277