Hayflick SJ (2007). "Neurodegeneration with brain iron accumulation: from genes to pathogenesis". Seminars in Pediatric Neurology. 13 (3): 182–5.
doi:
10.1016/j.spen.2006.08.007.
PMID17101457.
Johnson MA, Kuo YM, Westaway SK, et al. (2004). "Mitochondrial localization of human PANK2 and hypotheses of secondary iron accumulation in pantothenate kinase-associated neurodegeneration". Ann. N. Y. Acad. Sci. 1012 (1): 282–98.
Bibcode:
2004NYASA1012..282J.
doi:
10.1196/annals.1306.023.
PMID15105273.
S2CID29442698.
Yamashita S, Maeda Y, Ohmori H, et al. (2005). "Pantothenate kinase-associated neurodegeneration initially presenting as postural tremor alone in a Japanese family with homozygous N245S substitutions in the pantothenate kinase gene". J. Neurol. Sci. 225 (1–2): 129–33.
doi:
10.1016/j.jns.2004.07.012.
PMID15465096.
S2CID12640184.
Klopstock T, Elstner M, Lücking CB, et al. (2005). "Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease". Neurosci. Lett. 379 (3): 195–8.
doi:
10.1016/j.neulet.2004.12.061.
PMID15843062.
S2CID31733534.
Hayflick SJ (2007). "Neurodegeneration with brain iron accumulation: from genes to pathogenesis". Seminars in Pediatric Neurology. 13 (3): 182–5.
doi:
10.1016/j.spen.2006.08.007.
PMID17101457.
Johnson MA, Kuo YM, Westaway SK, et al. (2004). "Mitochondrial localization of human PANK2 and hypotheses of secondary iron accumulation in pantothenate kinase-associated neurodegeneration". Ann. N. Y. Acad. Sci. 1012 (1): 282–98.
Bibcode:
2004NYASA1012..282J.
doi:
10.1196/annals.1306.023.
PMID15105273.
S2CID29442698.
Yamashita S, Maeda Y, Ohmori H, et al. (2005). "Pantothenate kinase-associated neurodegeneration initially presenting as postural tremor alone in a Japanese family with homozygous N245S substitutions in the pantothenate kinase gene". J. Neurol. Sci. 225 (1–2): 129–33.
doi:
10.1016/j.jns.2004.07.012.
PMID15465096.
S2CID12640184.
Klopstock T, Elstner M, Lücking CB, et al. (2005). "Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease". Neurosci. Lett. 379 (3): 195–8.
doi:
10.1016/j.neulet.2004.12.061.
PMID15843062.
S2CID31733534.