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bibliographicCitation Havali C, Dorum S, Akbaş Y, Görükmez O, Hirfanoglu T. Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation. J Pediatr Endocrinol Metab. 2020 Mar 26;33(3):437–41. doi: 10.1515/jpem-2019-0194. PMID: 32069232.
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title Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation
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