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
Crossref DOI link: https://doi.org/10.1186/s12920-022-01159-2
Published Online: 2022-01-18
Published Print: 2022-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Dhangar, Somprakash
Panchal, Purvi
Ghatanatti, Jagdeeshwar
Suralkar, Jitendra
Shah, Anjali
Vundinti, Babu Rao https://orcid.org/0000-0003-4783-2691
Text and Data Mining valid from 2022-01-18
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Article History
First Online: 18 January 2022