whole-exome sequencing (wes)

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IFNAR1 gene mutation may contribute to developmental stuttering in the Chinese population.
Sun, Yimin;Gao, Yong;Zhou, Yuxi;Zhou, Yulong;Zhang, Ying;Wang, Dong;Tan, Li-Hai;
2021 Hereditas DOI: 10.1186/s41065-021-0... 249 views

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Hereditas
ISSN: 0018-0661 523 views

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