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Article

Ratbi, I, Falkenberg, KD, Sommen, M et al. (28 more authors) (2015) Heimler Syndrome is Caused by Hypomorphic Mutations in the Peroxisome Biogenesis Genes PEX1 and PEX6. American Journal of Human Genetics, 97. 1 - 11. ISSN 0002-9297

This list was generated on Sun Oct 20 21:39:55 2019 BST.