BMC Medical Genomics (Jan 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

  • Somprakash Dhangar,
  • Purvi Panchal,
  • Jagdeeshwar Ghatanatti,
  • Jitendra Suralkar,
  • Anjali Shah,
  • Babu Rao Vundinti

DOI
https://doi.org/10.1186/s12920-022-01159-2
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 3

Abstract

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