Additional file 1 of A de novo heterozygous variant in ACOX1 gene cause Mitchell syndrome: the first case in China and literature review
Autor: | Shen, Mengxiao, Chen, Qian, Gao, Yanyan, Yan, Hongyu, Feng, Shuo, Ji, Xinna, Zhang, Xue |
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Rok vydání: | 2023 |
DOI: | 10.6084/m9.figshare.23621340.v1 |
Popis: | Additional file 1: Table S1. Normal VLCFA levels are observed in our proband. |
Databáze: | OpenAIRE |
Externí odkaz: |