Somprakash Dhangar, Purvi Panchal, Jagdeeshwar Ghatanatti, Jitendra Suralkar, Anjali Shah, & Babu Rao Vundinti. (2022). 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. BMC.
Chicago Style (17th ed.) CitationSomprakash Dhangar, Purvi Panchal, Jagdeeshwar Ghatanatti, Jitendra Suralkar, Anjali Shah, and Babu Rao Vundinti. 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. BMC, 2022.
MLA (9th ed.) CitationSomprakash Dhangar, et al. 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. BMC, 2022.