Title : XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia.

Pub. Date : 2017 Jan 5

PMID : 28002403






1 Functional Relationships(s)
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1 Cells from a patient with mutations in XRCC1 exhibited not only reduced rates of single-strand break repair but also elevated levels of protein ADP-ribosylation. Adenosine Diphosphate X-ray repair cross complementing 1 Homo sapiens