Clinical exome sequencing reveals a mutation in PDHA1 in Leigh syndrome: A case of a Chinese boy with lethal neuropathy.
| Autor: | Gong, Ke1 (AUTHOR), Xie, Li1 (AUTHOR), Wu, Zhong‐shi1 (AUTHOR), Xie, Xia1 (AUTHOR), Zhang, Xing‐xing2 (AUTHOR), Chen, Jin‐Lan1 (AUTHOR) jinlanchen@csu.edu.cn |
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| Zdroj: | Molecular Genetics & Genomic Medicine. Apr2021, Vol. 9 Issue 4, p1-11. 11p. |
| Databáze: | Academic Search Ultimate |
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