Whole exome sequencing identified a novel nonsense INPP4A...

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European Journal of Medical Genetics 2020 / 1

Whole exome sequencing identified a novel nonsense INPP4A mutation in a family with intellectual disability

Banihashemi, Sara, Tahmasebi-Birgani, Maryam, Mohammadiasl, Javad, Hajjari, Mohammadreza
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Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2020.103846
Date:
January, 2020
File:
PDF, 838 KB
2020
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