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Article

Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.

International journal of laboratory hematology - 1 Oct 2020

Tavasoli Behnaz, Safa Majid, Dorgalaleh Akbar, Ghasemi Jahan B, Rezaei Makhouri Farahnaz, Rezvani Mohammad R, Ahmadi Abbas, Tabibian Shadi, Jazebi Mohammad, Baghaipour Mohammad R, Zaker Farhad

Abstract excerpt

INTRODUCTION: Congenital fibrinogen disorders (CFDs) comprise the quantitative and qualitative fibrinogen molecule abnormalities that are caused by fibrinogen gene mutations. The objective of this cohort research was to study the molecular and clinical profiles of patients with CFDs. MATERIALS AND METHODS: Genomic DNA Sanger sequencing of 14 Iranian patients was performed to determine CFDs-causing mutations. The...

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PMID: 32639687
DOI: 10.1111/ijlh.13258

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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