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Autor:
Blakes, Alexander JM, Wai, Htoo A, Davies, Ian, Moledina, Hassan E, Ruiz, April, Thomas, Tessy, Bunyan, David, Thomas, N Simon, Burren, Christine P, Greenhalgh, Lynn, Lees, Melissa, Pichini, Amanda, Smithson, Sarah F, Taylor Tavares, Ana Lisa, O'Donovan, Peter, Douglas, Andrew GL, Genomics England Research Consortium, Splicing, Whiffin, Nicola, Baralle, Diana, Lord, Jenny
Funder: Wessex Medical Research
Funder: Health Education England
Funder: Rosetrees Trust
BACKGROUND: Genomic variants which disrupt splicing are a major cause of rare genetic diseases. However, variants which lie outside of the canonic
Funder: Health Education England
Funder: Rosetrees Trust
BACKGROUND: Genomic variants which disrupt splicing are a major cause of rare genetic diseases. However, variants which lie outside of the canonic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ba3eb4525e0e70d291a5a83c537cd1e