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Verheij JB, Kunze J, Osinga J, van Essen AJ, Hofstra RM (2002). „ABCD syndrome is caused by a homozygous mutation in the EDNRB gene”. Am. J. Med. Genet.108 (3): 223–5. DOI:10.1002/ajmg.10172. PMID11891690.
Davenport AP (2002). „International Union of Pharmacology. XXIX. Update on endothelin receptor nomenclature”. Pharmacol. Rev.54 (2): 219–26. DOI:10.1124/pr.54.2.219. PMID12037137.
Verheij JB, Kunze J, Osinga J, van Essen AJ, Hofstra RM (2002). „ABCD syndrome is caused by a homozygous mutation in the EDNRB gene”. Am. J. Med. Genet.108 (3): 223–5. DOI:10.1002/ajmg.10172. PMID11891690.