Datta AK, Ghosh T, Nayak K, Ghosh M. Menkes kinky hair disease: A case report. „Cases J”. 1. 1, s. 158, 2008. DOI: 10.1186/1757-1626-1-158. PMID: 18801184.
Kim BE., Smith K., Meagher CK., Petris MJ. A conditional mutation affecting localization of the Menkes disease copper ATPase. Suppression by copper supplementation.. „The Journal of biological chemistry”. 46 (277), s. 44079–84, listopad 2002. DOI: 10.1074/jbc.M208737200. PMID: 12221109.
nih.gov
ncbi.nlm.nih.gov
Datta AK, Ghosh T, Nayak K, Ghosh M. Menkes kinky hair disease: A case report. „Cases J”. 1. 1, s. 158, 2008. DOI: 10.1186/1757-1626-1-158. PMID: 18801184.
Voskoboinik I., Camakaris J. Menkes copper-translocating P-type ATPase (ATP7A): biochemical and cell biology properties, and role in Menkes disease.. „Journal of bioenergetics and biomembranes”. 5 (34), s. 363–71, październik 2002. PMID: 12539963.
Kim BE., Smith K., Meagher CK., Petris MJ. A conditional mutation affecting localization of the Menkes disease copper ATPase. Suppression by copper supplementation.. „The Journal of biological chemistry”. 46 (277), s. 44079–84, listopad 2002. DOI: 10.1074/jbc.M208737200. PMID: 12221109.
Tønnesen T., Kleijer WJ., Horn N. Incidence of Menkes disease.. „Human genetics”. 4 (86), s. 408–10, luty 1991. PMID: 1999344.
Menkes JH, Alter M, Steigleder GK, Weakley DR, Sung JH. A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration. „Pediatrics”. 29, s. 764-79, 1962. PMID: 14472668.