Identification of Three Novel Mutations in the FANCA, FANCC, and ITGA2B Genes by Whole Exome Sequencing

BACKGROUND: Various blood diseases are caused by mutations in the FANCA, FANCC, and ITGA2B genes. Exome sequencing is a suitable method for identifying single-gene disease and genetic heterogeneity complaints. METHODS: Among families who were referred to Narges Genetic and PND Laboratory in 2015-201...

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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Int J Prev Med
Päätekijät: Negahdari, Samira, Zamani, Mina, Seifi, Tahereh, Sedighzadeh, Sahar, Mazaheri, Neda, Zeighami, Jawaher, Sedaghat, Alireza, Saberi, Alihossein, Hamid, Mohammad, keikhaei, Bijan, Radpour, Ramin, Shariati, Gholamreza, Galehdari, Hamid
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Wolters Kluwer - Medknow 2020
Aiheet:
Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7554563/
https://ncbi.nlm.nih.gov/pubmed/33088445
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijpvm.IJPVM_462_19
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