Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort

Overview of attention for article published in Frontiers in Genetics, April 2020

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Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort. https://t.co/XNow5ajhv1

16 May 2020

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Thanks @ItanLab. It was great to collaborate with you and your team for this article.

12 May 2020

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“Whole-exome and Sanger sequencing revealed 6 mutations in the TYR gene and 2 in the SLC45A2 gene, of which one was novel and two were described in a population study but were not previously associated with the OCA phenotype” -in a Brazilian cohort. Parabe

12 May 2020

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RT @ItanLab: Congrats @prandocarolina for the new article describing novel genetic variants underlying oculocutaneous albinism in a Brazili…

12 May 2020

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