TY  - GEN
AU  - Jungbluth,Heinz
AU  - Voermans,Nicol C
TI  - Congenital myopathies: not only a paediatric topic
SN  - 1473-6551
PY  - 2018///0109
KW  - Genotype
KW  - Humans
KW  - Muscle, Skeletal
KW  - pathology
KW  - Mutation
KW  - Myopathies, Structural, Congenital
KW  - diagnosis
KW  - Phenotype
KW  - Ryanodine Receptor Calcium Release Channel
KW  - genetics
N1  - Publication Type: Journal Article; Review
UR  - https://doi.org/10.1097/WCO.0000000000000372
ER  -