Identification of three novel mutations in the FANCA, FANCC, and ,ITGA2B genes by whole exome sequencing

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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Bibliographic Details
Main Authors: Samira Negahdari, Mina Zamani, Tahereh Seifi, Sahar Sedighzadeh, Neda Mazaheri, Jawaher Zeighami, Alireza Sedaghat, Alihossein Saberi, Mohammad Hamid, Bijan keikhaei, Ramin Radpour, Gholamreza Shariati, Hamid Galehdari
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:International Journal of Preventive Medicine
Subjects:
blood platelets
congenital abnormalities
dna
fanconi anemia
sequence analysis
Online Access:http://www.ijpvmjournal.net/article.asp?issn=2008-7802;year=2020;volume=11;issue=1;spage=117;epage=117;aulast=Negahdari

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http://www.ijpvmjournal.net/article.asp?issn=2008-7802;year=2020;volume=11;issue=1;spage=117;epage=117;aulast=Negahdari

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