Article
Screening for mutations in two exons of FANCG gene in Pakistani population.
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia - 1 Jun 2017
Aymun Ujala, Iram Saima, Aftab Iram, Khaliq Saba, Nadir Ali, Nisar Ahmed, Mohsin Shahida
Abstract excerpt
BACKGROUND: Fanconi anemia is a rare autosomal recessive disorder of genetic instability. It is both molecularly and clinically, a heterogeneous disorder. Its incidence is 1 in 129,000 births and relatively high in some ethnic groups. Sixteen genes have been identified among them mutations in FANCG gene are most common after FANCA and FANCC gene mutations. OBJECTIVE: To study mutations in exon 3 and 4 of FANCG...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.