Identification of a Novel Pathogenic Folliculin Variant in a Chinese Family With Birt–Hogg–Dubé Syndrome (Hornstein-Knickenberg Syndrome)
Author:
Publisher
Frontiers Media SA
Subject
Genetics(clinical),Genetics,Molecular Medicine
Reference37 articles.
1. Identification of a novel protein truncating mutation p.Asp98* in XPC associated with xeroderma pigmentosum in a consanguineous Pakistani family;Ali;Mol. Genet. Genomic Med.,2020
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3. Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons;Birt;Arch. Dermatol.,1977
4. Mesenchymal folliculin is required for alveolar development: implications for cystic lung disease in Birt-Hogg-Dube syndrome;Chu;Thorax,2020
5. Birt-Hogg-Dube syndrome-associated renal cell carcinoma: histopathological features and diagnostic conundrum;Furuya;Cancer Sci.,2020
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1. A Novel FLCN Variant in a Suspected Birt–Hogg–Dubè Syndrome Patient;International Journal of Molecular Sciences;2023-08-04
2. Outstanding Characteristics of Birt–Hogg–Dube Syndrome in Korea;Diagnostics;2023-06-13
3. Clinical and Genetic Comparison of Birt–Hogg–Dubé Syndrome (Hornstein–Knickenberg Syndrome) in Chinese: A Systemic Review of Reported Cases;International Journal of General Medicine;2022-05
4. Birt–Hogg–Dubé syndrome in Chinese patients: a literature review of 120 families;Orphanet Journal of Rare Diseases;2021-05-17
5. Molecular Dynamics of Mosquito-Plasmodium vivaxInteraction: A Smart Strategy of Parasitism;Cell Interaction - Molecular and Immunological Basis for Disease Management;2021-04-07
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