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Publications by Neslihan Önenli-Mungan

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

Internal Medicine

Molecular Biology

English

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Arylsulfatase B Deficiency in Maroteaux-Lamy Syndrome: Cellular Studies and Carrier Identification

Pediatric Research

English

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

Journal of Human Genetics

English

A Novel Mutation of the Arylsulfatase a Gene in Late-Onset Metachromatic Leukodystrophy

Journal of Clinical Psychiatry

English

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

Neurobiology of Aging

Developmental Biology

English

A Novel Missense Mutation of F 9 Gene in Hemophilia B Patients

Journal of Blood Disorders & Transfusion

English

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

Diagnostic Pathology

Forensic Medicine

English

Mitral Stenosis in the Maroteaux-Lamy Syndrome: A Treatable Cause of Dyspnoea.

Postgraduate Medical Journal

English

Diagnosis of Maroteaux—Lamy Syndrome by the Use of Radiolabelled Oligosaccharides as Substrates for the Determination of Arylsulphatase B Activity

Biochemical Journal

Molecular Biology

English

Mediterranean Fever Gene Mutation Analysis in Infertile Turkish Males

Genetics and Molecular Research

Molecular Biology

English