Literature

Main PEX26-F51L Paper

Tanaka, Okumoto, Tamura, Abe, Hirsch, Deng, Ekstein, Chung & Fujiki (2019). A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorder. Cold Spring Harbor Molecular Case Studies.

Citations

Papers citing the original PEX26-F51L report, fetched live from Semantic Scholar.

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