FANCA Gene Mutations in North African Fanconi Anemia Patients

Populations in North Africa (NA) are characterized by a high rate of consanguinity. Consequently, the proportion of founder mutations might be higher than expected and could be a major cause for the high prevalence of recessive genetic disorders like Fanconi anemia (FA). We report clinical, cytogene...

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Detalles Bibliográficos
Autores principales: Ben Haj Ali, Abir, Messaoud, Olfa, Elouej, Sahar, Talmoudi, Faten, Ayed, Wiem, Mellouli, Fethi, Ouederni, Monia, Hadiji, Sondes, De Sandre-Giovannoli, Annachiara, Delague, Valérie, Lévy, Nicolas, Bogliolo, Massimo, Surrallés, Jordi, Abdelhak, Sonia, Amouri, Ahlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933650/
https://www.ncbi.nlm.nih.gov/pubmed/33679882
http://dx.doi.org/10.3389/fgene.2021.610050

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933650/
https://www.ncbi.nlm.nih.gov/pubmed/33679882
http://dx.doi.org/10.3389/fgene.2021.610050

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