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An axonal Charcot-Marie-Tooth disease associated with a homozygous GDAP1 gene mutation in two siblings from Bangladesh: a less severe phenotype.
- Source :
-
Acta neurologica Belgica [Acta Neurol Belg] 2022 Jun; Vol. 122 (3), pp. 841-842. Date of Electronic Publication: 2022 Mar 22. - Publication Year :
- 2022
Details
- Language :
- English
- ISSN :
- 2240-2993
- Volume :
- 122
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Acta neurologica Belgica
- Publication Type :
- Editorial & Opinion
- Accession number :
- 35316520
- Full Text :
- https://doi.org/10.1007/s13760-022-01884-6