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Homozygous Mutation in the FANCD2 Gene Observed in a Saudi Male Infant with Severe Ambiguous Genitalia

Fanconi anemia (FA) is a rare autosomal recessive inherited disease caused by gene mutations that are primarily involved in the response to or repair of DNA damage. FA characterizes by multiple congenital abnormalities and malformations including growth retardation, renal agenesis, absence of radial...

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Bibliografske podrobnosti
izdano v:Case Rep Endocrinol
Main Authors: Al Jabri, Aida, Al Naim, Nusaybah, Al Dossari, Abeer
Format: Artigo
Jezik:Inglês
Izdano: Hindawi 2021
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8302383/
https://ncbi.nlm.nih.gov/pubmed/34327028
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/6686312
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