Contraction or sequence variant of an intergenic repeat-Alu element leads to inherited thyroid disease
Nat Genet
.
2024 May;56(5):738-739.
doi: 10.1038/s41588-024-01723-9.
Authors
Andrea Cortese
1
2
,
Elisa Vegezzi
3
,
Henry Houlden
4
Affiliations
1
Department of Neuromuscular Diseases, UCL Institute of Neurology, London, UK. andrea.cortese@ucl.ac.uk.
2
Department of Brain and Behaviour Sciences, University of Pavia, Pavia, Italy. andrea.cortese@ucl.ac.uk.
3
IRCCS Mondino Foundation, Pavia, Italy.
4
Department of Neuromuscular Diseases, UCL Institute of Neurology, London, UK.
PMID:
38714867
DOI:
10.1038/s41588-024-01723-9
No abstract available
Publication types
Letter
MeSH terms
DNA, Intergenic / genetics
Humans
Thyroid Diseases* / genetics
Grants and funding
MR/T001712/1/RCUK | Medical Research Council (MRC)
2019-1836/Fondazione Cariplo (Cariplo Foundation)