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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

Hutchin, TP, Navarro-Coy, NC orcid.org/0000-0002-1516-0571, Van Camp, G et al. (6 more authors) (2001) Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction. European Journal of Human Genetics, 9 (5). pp. 385-387. ISSN 1018-4813

This list was generated on Sun Oct 13 01:35:45 2019 BST.