Article ID Journal Published Year Pages File Type
5502504 Journal of the Neurological Sciences 2017 4 Pages PDF
Abstract
This is the first quantitative report presenting with the progression of brain atrophy in patients with XP-A. It is revealed that the brain atrophy started from early childhood in Japanese patients with XP-A carrying the homozygous founder mutation.
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Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
Preview
Quantitative analysis of brain atrophy in patients with xeroderma pigmentosum group A carrying the founder mutation in Japan
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