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Biallelic LINE insertion mutation in HACD1 causing congenital myopathy.
- Source :
-
Neurology. Genetics [Neurol Genet] 2020 Apr 13; Vol. 6 (3), pp. e423. Date of Electronic Publication: 2020 Apr 13 (Print Publication: 2020). - Publication Year :
- 2020
Details
- Language :
- English
- ISSN :
- 2376-7839
- Volume :
- 6
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Neurology. Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 32426512
- Full Text :
- https://doi.org/10.1212/NXG.0000000000000423