Williams-Beuren Syndrome Related Methyltransferase WBSCR27: From Structure to Possible Function

Williams-Beuren syndrome (WBS) is a genetic disorder associated with the hemizygous deletion of several genes in chromosome 7, encoding 26 proteins. Malfunction of these proteins induce multisystemic failure in an organism. While biological functions of most proteins are more or less established, th...

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Detalles Bibliográficos
Autores principales: Mariasina, Sofia S., Chang, Chi-Fon, Navalayeu, Tsimafei L., Chugunova, Anastasia A., Efimov, Sergey V., Zgoda, Viktor G., Ivlev, Vasily A., Dontsova, Olga A., Sergiev, Petr V., Polshakov, Vladimir I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Molecular Biosciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240639/
https://www.ncbi.nlm.nih.gov/pubmed/35782865
http://dx.doi.org/10.3389/fmolb.2022.865743

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240639/
https://www.ncbi.nlm.nih.gov/pubmed/35782865
http://dx.doi.org/10.3389/fmolb.2022.865743

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