Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Analysis of clinical, gene mutation characteristics, and treatment prognosis of type 2A hereditary hemochromatosis in the Chinese population].

Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology - 20 Nov 2024

Zhang W, Li Y M, Xu A J, Wang X M, Wang Y, Duan W J, Zhao X Y, Xu H X, Jiang J P, Jiang W, Huang J, Ou X J

Abstract excerpt

Objective: To analyze the clinical, genetic mutation characteristics, and treatment prognosis of type 2A hereditary hemochromatosis (HH) in China. Methods: Peripheral blood samples and clinical data of patients with primary iron overload were collected through the China Registry of Genetic/Metabolic Liver Disease from June 2015 to November 2023. HH-related genes were detected by Sanger sequencing. Clinical...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to China
Share to East Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ferritins

Share to GPI-Linked Proteins

Share to Hemochromatosis

Share to Hemochromatosis Protein

Share to Iron Overload

Share to Prognosis

Source

Open in PubMed Open full text

Identifiers

PMID: 39623577
DOI: 10.3760/cma.j.cn501113-20231207-00271
PMCID: PMC12899067

Genes

HJV

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Analysis of clinical, gene mutation characteristics, and treatment prognosis of type 2A hereditary hemochromatosis in the Chinese population].PMID 39623577Read ↗

Correlation of Genotype and Phenotype in 32 Patients with Hereditary Hemochromatosis in ChinaSemantic proximity Read ↗

[Hemochromatosis International: therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr homozygous genotype].Semantic proximity Read ↗

Iranian hereditary hemochromatosis patients: baseline characteristics, laboratory data and gene mutations.Semantic proximity Read ↗

[Mutation analysis of the pathogenic gene in a Chinese family with hereditary hemochromatosis].Semantic proximity Read ↗

Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China.Semantic proximity Read ↗

Diagnosis and Management of Non-HFE Hemochromatosis, Ferroportin Disease, and Rare Hereditary Iron-Loading Disorders.Semantic proximity Read ↗

SLC40A1-related hemochromatosis associated with a p.Y333H mutation in mainland China: a pedigree report and literature review.Semantic proximity Read ↗

EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)Semantic proximity Read ↗

HFE-associated hereditary hemochromatosis: overview of genetics and clinical implications for nurse practitioners in primary care settings.Semantic proximity Read ↗

[Genotype-phenotype relationship and genetics study of 115 cases with Wilson's disease].Semantic proximity Read ↗

Hereditary HemochromatosisSemantic proximity Read ↗

Hereditary hemochromatosis: pathophysiology, diagnosis, and management.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.