Mehri Khatami
Department of Biology, Faculty of science, Yazd University, Yazd, Iran.Yazd, Iran
Abstracts, Mehri Khatami [Author]
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Novel and Heteroplasmic Mutations in Mitochondrial Coding Genes in Iranian Patients with Familial Adenomatous Polyposis (FAP)
Medical GeneticsFamilial Adenomatous Polyposis (FAP) is an Autosomal dominant inherited disorder and a rare form of colorectal cance...Read more
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A Novel Missense Mutation (G106R) in Thyroid Stimulating Hormone β-subunit gene in Patients with Central Congenital Hypothyroidism
Metabolism and Metabolic DiseasesBackground: Central Congenital hypothyroidism (CCH) is a rare and evades diagnosis on thyroid stimulating hormone (TSH)-...Read more
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Identification of Heterozygote Mutations in Exon 1 of NKX2.1 Gene in Patients with Congenital Hypothyroidism
Metabolism and Metabolic DiseasesIntroduction: Congenital hypothyroidism (CH) is a most common congenital endocrine disorder, affecting 1 in 3000 to 4000...Read more