Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Rebekah, Kember"'
Autor:
Steven Erwood, Elzbieta Hyatt, Madeleine Durbeej, Prabhpreet S Bassi, Dwi U. Kemaladewi, Dhekra Al-Basha, Kara M Place, Evgueni A. Ivakine, R. Marks, Ronald D. Cohn, Lindsay K, Steven A. Prescott, Rebekah Kember, Kinga I. Gawlik
Publikováno v:
Nature. 572:125-130
Neuromuscular disorders are often caused by heterogeneous mutations in large, structurally complex genes. Targeting compensatory modifier genes could be beneficial to improve disease phenotypes. Here we report a mutation-independent strategy to upreg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5d4a484017822250760e2347c25f3f9
https://doi.org/10.1038/s41586-019-1430-x
https://doi.org/10.1038/s41586-019-1430-x
Autor:
Dwi U, Kemaladewi, Prabhpreet S, Bassi, Steven, Erwood, Dhekra, Al-Basha, Kinga I, Gawlik, Kyle, Lindsay, Elzbieta, Hyatt, Rebekah, Kember, Kara M, Place, Ryan M, Marks, Madeleine, Durbeej, Steven A, Prescott, Evgueni A, Ivakine, Ronald D, Cohn
Publikováno v:
Nature. 572(7767)
Neuromuscular disorders are often caused by heterogeneous mutations in large, structurally complex genes. Targeting compensatory modifier genes could be beneficial to improve disease phenotypes. Here we report a mutation-independent strategy to upreg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05401e630c5ccf47f1b1374efb085b8b
https://pubmed.ncbi.nlm.nih.gov/31341277
https://pubmed.ncbi.nlm.nih.gov/31341277