TY  - GEN
AU  - Findlay,Andrew R
AU  - Harms,Matthew B
AU  - Pestronk,Alan
AU  - Weihl,Conrad C
TI  - Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy
SN  - 1873-2364
PY  - 2019///1023
KW  - Adult
KW  - Humans
KW  - Male
KW  - Muscle Weakness
KW  - genetics
KW  - Muscle, Skeletal
KW  - pathology
KW  - Muscular Diseases
KW  - Mutation, Missense
KW  - Myosin Heavy Chains
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.nmd.2018.05.006
ER  -