Proceedings of a Sickle Cell Disease Ontology workshop — Towards the first comprehensive ontology for Sickle Cell Disease

Sickle cell disease (SCD) is a debilitating single gene disorder caused by a single point mutation that results in physical deformation (i.e. sickling) of erythrocytes at reduced oxygen tensions. Up to 75% of SCD in newborns world-wide occurs in sub-Saharan Africa, where neonatal and childhood morta...

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Detalles Bibliográficos
Autores principales: Mulder, Nicola, Nembaware, Victoria, Adekile, Adekunle, Anie, Kofi A., Inusa, Baba, Brown, Biobele, Campbell, Andrew, Chinenere, Furahini, Chunda-Liyoka, Catherine, Derebail, Vimal K., Geard, Amy, Ghedira, Kais, Hamilton, Carol M., Hanchard, Neil A., Haendel, Melissa, Huggins, Wayne, Ibrahim, Muntaser, Jupp, Simon, Kamga, Karen Kengne, Knight-Madden, Jennifer, Lopez-Sall, Philomène, Mbiyavanga, Mamana, Munube, Deogratias, Nirenberg, Damian, Nnodu, Obiageli, Ofori-Acquah, Solomon Fiifi, Ohene-Frempong, Kwaku, Opap, Kenneth Babu, Panji, Sumir, Park, Miriam, Pule, Gift, Royal, Charmaine, Sangeda, Raphael, Tayo, Bamidele, Treadwell, Marsha, Tshilolo, Léon, Wonkam, Ambroise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911424/
https://www.ncbi.nlm.nih.gov/pubmed/27354937
http://dx.doi.org/10.1016/j.atg.2016.03.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911424/
https://www.ncbi.nlm.nih.gov/pubmed/27354937
http://dx.doi.org/10.1016/j.atg.2016.03.005

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