BMC Med Genomics
 2022
DOI: 10.1186/s12920-022-01159-2
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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 Dhangar
1
,
Purvi Panchal
2
,
Jagdeeshwar Ghatanatti
3
et al.
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