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Publications by F.-J. Tsai

Molecular Analysis of Wilson Disease in Taiwan: Identification of One Novel Mutation and Evidence of Haplotype-Mutation Association

Journal of Human Genetics

Genetics

2000

English

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Progranulin Mutation Analysis: Identification of One Novel Mutation in Exon 12 Associated With Frontotemporal Dementia

Neurobiology of Aging

Aging

Gerontology

Developmental Biology

English

Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB) Gene

English

Molecular Analysis of Mucopolysaccharidosis Type I in Tunisia: Identification of Novel Mutation and Eight Novel Polymorphisms

English

Mutation Analysis of 73 Southern Chinese Wilson's Disease Patients: Identification of 10 Novel Mutations and Its Clinical Correlation

Journal of Human Genetics

Genetics

2011

English

Mutation Analysis of the SDHB and SDHD Genes in Pheochromocytomas and Paragangliomas: Identification of a Novel Nonsense Mutation (Q168X) in the SDHB Gene

English

IL2RG Hypomorphic Mutation: Identification of a Novel Pathogenic Mutation in Exon 8 and a Review of the Literature

Allergy, Asthma and Clinical Immunology

English

Identification and Functional Analysis of a Novel Von Willebrand Factor Mutation in a Family With Type 2A Von Willebrand Disease

PLoS ONE

Multidisciplinary

2012

English

Identification of Key Pathways and Genes in TP53 Mutation Acute Myeloid Leukemia: Evidence From Bioinformatics Analysis

OncoTargets and Therapy

Oncology

Pharmacology

2017

English

Intragenic Deletion as a Novel Type of Mutation in Wolman Disease

Molecular Genetics and Metabolism

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by F.-J. Tsai

Molecular Analysis of Wilson Disease in Taiwan: Identification of One Novel Mutation and Evidence of Haplotype-Mutation Association

Related publications

Progranulin Mutation Analysis: Identification of One Novel Mutation in Exon 12 Associated With Frontotemporal Dementia

Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB) Gene

Molecular Analysis of Mucopolysaccharidosis Type I in Tunisia: Identification of Novel Mutation and Eight Novel Polymorphisms

Mutation Analysis of 73 Southern Chinese Wilson's Disease Patients: Identification of 10 Novel Mutations and Its Clinical Correlation

Mutation Analysis of the SDHB and SDHD Genes in Pheochromocytomas and Paragangliomas: Identification of a Novel Nonsense Mutation (Q168X) in the SDHB Gene

IL2RG Hypomorphic Mutation: Identification of a Novel Pathogenic Mutation in Exon 8 and a Review of the Literature

Identification and Functional Analysis of a Novel Von Willebrand Factor Mutation in a Family With Type 2A Von Willebrand Disease

Identification of Key Pathways and Genes in TP53 Mutation Acute Myeloid Leukemia: Evidence From Bioinformatics Analysis

Intragenic Deletion as a Novel Type of Mutation in Wolman Disease