Browse by UCL people
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Number of items: 2.
Article
Cortese, A;
Simone, R;
Sullivan, R;
Vandrovcova, J;
Tariq, H;
Yan, YW;
Humphrey, J;
... Houlden, H; + view all
(2019)
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.
Nature Genetics
, 51
(4)
pp. 649-658.
10.1038/s41588-019-0372-4.
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Tariq, H;
Butt, JUR;
Houlden, H;
Naz, S;
(2019)
Are some C19orf12 variants monoallelic for neurological disorders?
Parkinsonism & Related Disorders
, 65
pp. 267-269.
10.1016/j.parkreldis.2019.05.020.
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