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 Med Genomics. 2022 Jan 18;15(1):11.
doi: 10.1186/s12920-022-01159-2.
1 Department of Cytogenetics, National Institute of Immunohaematology (ICMR), 13th Floor, New Multistoried Building, K.E.M Hospital Campus, Parel, Mumbai, 400012, India.
2 Department of Cytogenetics, National Institute of Immunohaematology (ICMR), 13th Floor, New Multistoried Building, K.E.M Hospital Campus, Parel, Mumbai, 400012, India. vbaburao@hotmail.com.