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
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