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pro vyhledávání: '"Oumaima, Chargui"'
Autor:
Virginie, Marty, Jasmine, Butler, Coutens, Basile, Oumaima, Chargui, Abdeslam, Chagraoui, Bruno P, Guiard, Philippe, De Deurwaerdère, Jérôme, Cavaillé
Publikováno v:
Human Molecular Genetics. 32:244-261
The neuronal-specific SNORD115 has gathered interest because its deficiency may contribute to the pathophysiology of Prader-Willi syndrome (PWS), possibly by altering post-transcriptional regulation of the gene encoding the serotonin (HTR2C) receptor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b79422b39db7580d394576a008ba3b7
https://doi.org/10.1093/hmg/ddac139
https://doi.org/10.1093/hmg/ddac139
