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 2024/04/24
AB Rare,  congenital,  slowly  progressive  inherited  neuromuscular  disease  that  usually  is  apparent  at  birth;  characterized  by  extreme  hypotonia.