Fletcher, N.
Walton Centre
2 papers on CoChatORCID 0000-0001-5146-8891
Most cited papers
- Verified
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation
Chinnery, P. F., Crompton, D. E., Birchall, D., Jackson, M. J., Coulthard, A., Lombes, A., Quinn, N., Wills, A., Fletcher, N., Mottershead, J. P., et al. (2006) · Brain
Neurological diseases and metabolismParkinson's Disease Mechanisms and Treatments
Cited by 205
- Verified
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts
Jenkinson, E. M., Rodero, M. P., Kasher, P. R., Uggenti, C., Oojageer, A., Goosey, L. C., Rose, Y., Kershaw, C. J., Urquhart, J. E., Williams, S. G., et al. (2016) · Nature Genetics
Cerebrovascular and genetic disordersGenomics and Rare Diseases
Cited by 148
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