RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58081489 T1 Nemaline Rod Myopathy T2 Syndromes: Rapid Recognition and Perioperative Implications YR 2006 FD 2006 PB The McGraw-Hill Companies PP New York, NY SN 9780071354554 LK accessanesthesiology.mhmedical.com/content.aspx?aid=58081489 RD 2024/10/15 AB Rare, congenital, slowly progressive inherited neuromuscular disease that usually is apparent at birth; characterized by extreme hypotonia.