Novel PEX1 mutations in fibroblasts from children with Zellweger spectrum disorders exhibit temperature sensitive characteristics
Author:
Publisher
Elsevier BV
Subject
Behavioral Neuroscience,Neurology (clinical),Neurology
Reference42 articles.
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3. Spectrum of PEX1 and PEX6 variants in Heimler syndrome;Smith;Eur J Hum Genet,2016
4. Heimler syndrome is caused by hypomorphic mutations in the peroxisome-biogenesis genes PEX1 and PEX6;Ratbi;Am J Hum Genet,2015
5. Peroxisome: Metabolic Functions and Biogenesis;Okumoto,2020
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