For: | Ding L, Huang TT, Ying GH, Wang SY, Xu HF, Qian H, Rahman F, Lu XP, Guo H, Zheng G, Zhang G. De novo mutation of NAXE (APOAIBP)-related early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy-1: A case report. World J Clin Cases 2023; 11(14): 3340-3350 [PMID: 37274027 DOI: 10.12998/wjcc.v11.i14.3340] |
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URL: | https://www.wjgnet.com/2307-8960/full/v11/i14/3340.htm |
Number | Citing Articles |
1 |
Boraan Abdulkarim, Setu Mittal, Hassan Vahidnezhad, Dawn Marie Davis, Michael J. Camilleri, Nessa Aghazadeh Mohandesi. Cutaneous Manifestations of NAXD or NAXE Deficiency: A Literature Review for the Dermatologist. Pediatric Dermatology 2025; 42(2): 233 doi: 10.1111/pde.15868
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2 |
Kokoro Ozaki, Yukiko Yatsuka, Yoshinobu Oyazato, Atsushi Nishiyama, Kazuhiro R. Nitta, Yoshihito Kishita, Takuya Fushimi, Masaru Shimura, Shohei Noma, Yohei Sugiyama, Michihira Tagami, Moe Fukunaga, Hiroko Kinoshita, Tomoko Hirata, Wataru Suda, Yasuhiro Murakawa, Piero Carninci, Akira Ohtake, Kei Murayama, Yasushi Okazaki. Biallelic GGGCC repeat expansion leading to NAXE-related mitochondrial encephalopathy. npj Genomic Medicine 2024; 9(1) doi: 10.1038/s41525-024-00429-5
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