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Publications by Florian Gundel

A New Ankyrin Mutation (ANK1 EXON E9X) Causing Severe Hereditary Spherocytosis in the Neonatal Period

Annals of Hematology

English

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An ANK1 IVS3-2A>C Mutation Causes Exon 4 Skipping in Two Patients From a Chinese Family With Hereditary Spherocytosis

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Novel Hereditary Spherocytosis-Associated Splice Site Mutation in the ANK1 Gene Caused by Parental Gonosomal Mosaicism

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Targeted Next-Generation Sequencing Identified a Novel ANK1 Mutation Associated With Hereditary Spherocytosis in a Chinese Family

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Hereditary Spherocytosis; New Guidelines

Archives of Disease in Childhood

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Erythrocyte Ankyrin Promoter Mutations Associated With Recessive Hereditary Spherocytosis Cause Significant Abnormalities in Ankyrin Expression

Journal of Biological Chemistry

Molecular Biology

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Exon 12 Ceruloplasmin Gene New Nonsense Mutation Causing Aceruloplasminemia in an Italian Patient

Open Journal of Internal Medicine

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Current Problems in Haematology. 2: Hereditary Spherocytosis.

Journal of Clinical Pathology

Forensic Medicine

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Clinical, Genetic, and Biophysical Characterization of a Homozygous HERG Mutation Causing Severe Neonatal Long QT Syndrome

Pediatric Research

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Genotype/Phenotype Correlation in Hereditary Spherocytosis

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