Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy

Detalles Bibliográficos
Autores principales: Salman, Mohd, Verma, Anshuman, Chaurasia, Sunita, Prasad, Deeksha, Kannabiran, Chitra, Singh, Vivek, Ramappa, Muralidhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311843/
https://www.ncbi.nlm.nih.gov/pubmed/37386499
http://dx.doi.org/10.1186/s13023-023-02791-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311843/
https://www.ncbi.nlm.nih.gov/pubmed/37386499
http://dx.doi.org/10.1186/s13023-023-02791-6

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