Correction to: Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations

Detalles Bibliográficos
Autores principales: Dhangar, Somprakash, Panchal, Purvi, Ghatanatti, Jagdeeshwar, Suralkar, Jitendra, Shah, Anjali, Vundinti, Babu Rao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767666/
https://www.ncbi.nlm.nih.gov/pubmed/35042536
http://dx.doi.org/10.1186/s12920-022-01159-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767666/
https://www.ncbi.nlm.nih.gov/pubmed/35042536
http://dx.doi.org/10.1186/s12920-022-01159-2

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