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Publications by Roland Zuest

Complete Human CD1a Deficiency on Langerhans Cells Due to a Rare Point Mutation in the Coding Sequence

Journal of Allergy and Clinical Immunology

English

Related publications

A Point Mutation in the VP4 Coding Sequence of Coxsackievirus B4 Influences Virulence.

Journal of Virology

English

Polyclonal T-Cells Express CD1a in Langerhans Cell Histiocytosis (LCH) Lesions

Multidisciplinary

English

Genetic Basis of Human Complement C4A Deficiency. Detection of a Point Mutation Leading to Nonexpression.

Journal of Clinical Investigation

English

Human Swayback Due to Copper Deficiency

The Internet Journal of Nutrition and Wellness

English

Coding-Complete Genome Sequence of a Recombinant Human Norovirus Strain Identified as Subtype GII.p12_GII.3

Microbiology Resource Announcements

Molecular Biology

English

Cytochrome C Oxidase Deficiency Associated With the First Stop-Codon Point Mutation in Human mtDNA

American Journal of Human Genetics

English

Complete Coding Sequence of Rat Tyrosine Hydroxylase mRNA.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

A Rare Cause of Primary Hypoparathyroidism Due to a Novel Mutation in the GATA3 Gene – The Barakat Syndrome

International Journal of Pediatric Endocrinology

English

Complete Nucleotide Sequence of a Gene Coding forAspergillus Aculeatuscellulase (FI-CMCase)

Nucleic Acids Research

English