Browse by UCL people
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Number of items: 2.
Article
Thomas, AC;
Williams, H;
Seto-Salvia, N;
Bacchelli, C;
Jenkins, D;
O'Sullivan, M;
Mengrelis, K;
... Stanier, PM; + view all
(2014)
Mutations in SNX14 cause a distinctive autosomal recessive cerebellar ataxia and intellectual disability syndrome.
The American Journal of Human Genetics
, 95
(5)
pp. 611-621.
10.1016/j.ajhg.2014.10.007.
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Thesis
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Mengrelis, K;
(2016)
The role of Hedgehog signalling in the homeostasis and differentiation of GammaDelta and AlphaBeta T cells.
Doctoral thesis , UCL (University College London).
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