Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract

PURPOSE: Introns play an important role in gene regulation and expression. Single nucleotide polymorphisms (SNPs) in introns have the potential to cause disease and alter the genotype–phenotype association. Hence, this study aimed to decipher the association of SNPs in the introns of the crystallin...

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Detalles Bibliográficos
Autores principales: Nair, Vidya, Sankaranarayanan, Rajkumar, Vasavada, Abhay Raghukant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482906/
https://www.ncbi.nlm.nih.gov/pubmed/34304179
http://dx.doi.org/10.4103/ijo.IJO_3062_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482906/
https://www.ncbi.nlm.nih.gov/pubmed/34304179
http://dx.doi.org/10.4103/ijo.IJO_3062_20

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