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

Overview of attention for article published in BMC Medical Genomics, January 2022

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https://t.co/asxCuwvHp2 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 https://t.co/eAKJTi6khz

03 Jan 2022

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