Associated Papers
Spectrum of genetic alterations in patients with peroxisome biogenesis defects in the Iranian population: a case series study.
Khalilian S et al.
Bmc Medical Genomics, 2025
A novel splice variant in intron 10 of PEX6 is associated with Zellweger Syndrome in a Chinese neonate.
Yang P et al.
Gene, 2024
[Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review].
Yang P et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2024
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