Clinical, neuroradiological, and molecular phenotyping of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations

Cheung, Anthony; Argyriou, Catherine; Yergeau, Christine; D'Souza, Yasmin; Riou, Émilie; Levesque, Sébastien; Raymond, G. S.; Daba, Mebratu; Rtskhiladze, Irakli; Tkemaladze, Tinatin; Adang, Laura; Piana, Roberta La; Bernard, Geneviève; Braverman, Nancy

doi:10.1016/s1096-7192(21)00088-3

Molecular Genetics and Metabolism

2021

DOI: 10.1016/s1096-7192(21)00088-3

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Clinical, neuroradiological, and molecular phenotyping of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations

Anthony Cheung¹,

Catherine Argyriou²,

Christine Yergeau³

et al.

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Clinical, neuroradiological, and molecular phenotyping of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations

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