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CONGENITAL MYOPATHIES: EP.52 Characterization of a novel mouse model carrying the homozygous p.F4976L RYR1 mutation, identified in a severely affected child.
- Source :
-
Neuromuscular Disorders . 2021 Supplement 1, Vol. 31, pS65-S65. 1p. - Publication Year :
- 2021
- Subjects :
- *LABORATORY mice
*ANIMAL disease models
*MUSCLE diseases
*NEMALINE myopathy
Subjects
Details
- Language :
- English
- ISSN :
- 09608966
- Volume :
- 31
- Database :
- Academic Search Index
- Journal :
- Neuromuscular Disorders
- Publication Type :
- Academic Journal
- Accession number :
- 152517109
- Full Text :
- https://doi.org/10.1016/j.nmd.2021.07.077