TY  - CHAP
M1  - Book, Section
TI  - Mitochondrial Disorders
A1  - Amato, Anthony A.
A1  - Russell, James A.
PY  - 2015
T2  - Neuromuscular Disorders, 2e
AB  - Mitochondrial  myopathies  and  neuropathies  or  neuromyopathies  refer  to  a  heterogeneous  group  of  disorders  caused  by  dysfunction  of  mitochondria.1–10  Mitochondrial  disorders  can  be  classified  according  to  the  associated  biochemical,  genetic  defects,  or  clinical  phenotype  (Tables  30-1,30-2,30-3).  One  difficulty  in  classifying  patients  by  any  particular  scheme  is  the  clinical-phenotypic  heterogeneity  associated  with  specific  mitochondrial  mutations  and  the  genetic  heterogeneity  in  well-defined  clinical  phenotypes  that  are  seen  with  mitochondrial  disorders.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/20
UR  - neurology.mhmedical.com/content.aspx?aid=1115662003
ER  -