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. 2022 Jul 8;13:884522. doi: 10.3389/fgene.2022.884522

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Copyright © 2022 Jin, Liu, Xie, Xie, Chen and Sun.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Genetic sequencing results of the probands and their parents. Mutated sequences of the identified c.997 G > A (A) and c.6603-3 T > G (B) variant. The red arrow indicates the site of the base deletion or substitution.