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Publications by Alan A. Wanderer

Mutation of a New Gene Encoding a Putative Pyrin-Like Protein Causes Familial Cold Autoinflammatory Syndrome and Muckle–Wells Syndrome

Nature Genetics

English

Familial Atypical Cold Urticaria: Description of a New Hereditary Disease

Journal of Allergy and Clinical Immunology

English

Related publications

Muckle–Wells Syndrome in a Child With Recurrent Urticaria

Voprosy Sovremennoi Pediatrii - Current Pediatrics

English

Genetic Linkage of the Muckle-Wells Syndrome to Chromosome 1q44

American Journal of Human Genetics

English

Mutation of an A-Kinase-Anchoring Protein Causes Long-Qt Syndrome

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

Multidisciplinary

English

A Post-Vaccination Autoinflammatory Syndrome

Research in Immunology: An International Journal

English

Mutation in a Putative Glycosyltransferase-Like Gene Causes Programmed Cell Death and Early Leaf Senescence in Rice

English

R231C Mutation in KCNQ1 Causes Long QT Syndrome Type 1 and Familial Atrial Fibrillation

Cardiovascular Medicine

English

A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report

Frontiers in Genetics

Molecular Medicine

English

A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English

A Familial Case of Nevoid Basal Cell Carcinoma Syndrome With a Frameshift Mutation in the PTCH1 Gene

Japanese Journal of Oral and Maxillofacial Surgery

English