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A lethal defect of mitochondrial and peroxisomal fission.
Waterham HR, Koster J, van Roermund CW, Mooyer PA, Wanders RJ, Leonard JV. Waterham HR, et al. Among authors: mooyer pa. N Engl J Med. 2007 Apr 26;356(17):1736-41. doi: 10.1056/NEJMoa064436. N Engl J Med. 2007. PMID: 17460227 Free article.
ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism.
Ferdinandusse S, Falkenberg KD, Koster J, Mooyer PA, Jones R, van Roermund CWT, Pizzino A, Schrader M, Wanders RJA, Vanderver A, Waterham HR. Ferdinandusse S, et al. Among authors: mooyer pa. J Med Genet. 2017 May;54(5):330-337. doi: 10.1136/jmedgenet-2016-104132. Epub 2016 Oct 31. J Med Genet. 2017. PMID: 27799409
Clinical and biochemical spectrum of D-bifunctional protein deficiency.
Ferdinandusse S, Denis S, Mooyer PA, Dekker C, Duran M, Soorani-Lunsing RJ, Boltshauser E, Macaya A, Gärtner J, Majoie CB, Barth PG, Wanders RJ, Poll-The BT. Ferdinandusse S, et al. Among authors: mooyer pa. Ann Neurol. 2006 Jan;59(1):92-104. doi: 10.1002/ana.20702. Ann Neurol. 2006. PMID: 16278854
A key role for the peroxisomal ABCD2 transporter in fatty acid homeostasis.
Fourcade S, Ruiz M, Camps C, Schlüter A, Houten SM, Mooyer PA, Pàmpols T, Dacremont G, Wanders RJ, Giròs M, Pujol A. Fourcade S, et al. Among authors: mooyer pa. Am J Physiol Endocrinol Metab. 2009 Jan;296(1):E211-21. doi: 10.1152/ajpendo.90736.2008. Epub 2008 Oct 14. Am J Physiol Endocrinol Metab. 2009. PMID: 18854420 Free article.
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