File:Fped-09-751895-g005.jpg

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English: The localization of 30 homozygous or compound heterozygous variants in ACSF3 reported worldwide (except for a Chr16:87441993:89171912 deletion spanning ACSF3). The types of the variants include missense, nonsense, deletion, frameshift, and splice site variants. The most common type is missense.
Date
Source https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658908/
Author Ping Wang, Jianbo Shu, Chunyu Gu, Xiaoli Yu, Jie Zheng, Chunhua Zhang, and Chunquan Cai

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current20:31, 13 July 2023Thumbnail for version as of 20:31, 13 July 2023957 × 356 (204 KB)Ozzie10aaaa (talk | contribs)Uploaded a work by Ping Wang, Jianbo Shu, Chunyu Gu, Xiaoli Yu, Jie Zheng, Chunhua Zhang, and Chunquan Cai from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658908/ with UploadWizard

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