TY  - CHAP
M1  - Book, Section
TI  - Nemaline Rod Myopathy
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Rare,  congenital,  slowly  progressive  inherited  neuromuscular  disease  that  usually  is  apparent  at  birth;  characterized  by  extreme  hypotonia.  No  evidence  for  susceptibility  for  malignant  hyperpyrexia.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/16
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164080106
ER  -