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Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
- Source :
- Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-1 (2023)
- Publication Year :
- 2023
- Publisher :
- BMC, 2023.
- Subjects :
- Medicine
Subjects
Details
- Language :
- English
- ISSN :
- 17501172
- Volume :
- 18
- Issue :
- 1
- Database :
- Directory of Open Access Journals
- Journal :
- Orphanet Journal of Rare Diseases
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.6f493be37abf4db98eec23b19fb26657
- Document Type :
- article
- Full Text :
- https://doi.org/10.1186/s13023-023-02791-6