Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate

The majority (85%) of nonsyndromic cleft lip with or without cleft palate (nsCL/P) cases occur sporadically, suggesting a role for de novo mutations (DNMs) in the etiology of nsCL/P. To identify high impact protein-altering DNMs that contribute to the risk of nsCL/P, we conducted whole-genome sequen...

Descripción completa

Detalles Bibliográficos
Autores principales: Awotoye, Waheed, Mossey, Peter A., Hetmanski, Jacqueline B., Gowans, Lord J. J., Eshete, Mekonen A., Adeyemo, Wasiu L., Alade, Azeez, Zeng, Erliang, Adamson, Olawale, Naicker, Thirona, Anand, Deepti, Adeleke, Chinyere, Busch, Tamara, Li, Mary, Petrin, Aline, Aregbesola, Babatunde S., Braimah, Ramat O., Oginni, Fadekemi O., Oladele, Ayodeji O., Oladayo, Abimbola, Kayali, Sami, Olotu, Joy, Hassan, Mohaned, Pape, John, Donkor, Peter, Arthur, Fareed K. N., Obiri-Yeboah, Solomon, Sabbah, Daniel K., Agbenorku, Pius, Plange-Rhule, Gyikua, Oti, Alexander Acheampong, Gogal, Rose A., Beaty, Terri H., Taub, Margaret, Marazita, Mary L., Schnieders, Michael J., Lachke, Salil A., Adeyemo, Adebowale A., Murray, Jeffrey C., Butali, Azeez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273634/
https://www.ncbi.nlm.nih.gov/pubmed/35817949
http://dx.doi.org/10.1038/s41598-022-15885-1

Ejemplares similares

Ejemplares similares