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.
Somprakash DhangarPurvi PanchalJagdeeshwar GhatanattiJitendra SuralkarAnjali ShahBabu Rao VundintiPublished in: BMC medical genomics (2022)