Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3

Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3–p13

Published:1996-12-01 Issue:4 Volume:14 Page:479-481
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Taylor Todd D.,Litt Michael,Kramer Patricia,Pandolfo Massimo,Angelini Lucia,Nardocci Nardo,Davis Suzanne,Pineda M.,Hattori Haruo,Flett Peter J.,Cilio M. Roberta,Bertini Enrico,Hayflick Susan J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1296-479.pdf

Reference35 articles.

1. Dooling, E.C., Schoene, W.C. & Richardson, E.P. Jr., Hallervorden-Spatz syndrome. Arch. Neurol. 30, 70–83 (1974).

2. Hill, J.M. & Switzer, R.C. The regional distribution and cellular localization of iron in the rat brain. Neuroscience 11, 595–603 (1984).

3. Sofic, E. et al. Increased iron III and total iron content in postmortem substantia nigra in parkinsonian brain. J. Neural Transmission 74, 199–205 (1988).

4. Riederer, P. et al. Transition metals, ferritin, glutathione and ascorbic acid in parkinsonian brains. J. Neurochem. 52, 515–520 (1989).

5. Connor, J.R., Snyder, B.S., Beard, J.L., Fine, R.E. & Mufson, E.J. Regional distribution of iron and iron regulatory proteins in the brain in aging and Alzheimer's disease. J. Neurosci. Res. 31, 327–335 (1992).

Cited by 134 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Neurodegeneration with Brain Iron Accumulation Disorders and Retinal Neurovascular Structure;Movement Disorders;2023-11-10

2. A Brief History of NBIA Gene Discovery;Journal of Movement Disorders;2023-05-31

3. NBIA Syndromes;Neurology India;2021-09

4. Dystonia;Principles and Practice of Movement Disorders;2021

5. Clinical overview and phenomenology of movement disorders;Principles and Practice of Movement Disorders;2021