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Publications by Robert Kleta

Risk HLA-DQA1 and PLA2R1 Alleles in Idiopathic Membranous Nephropathy

New England Journal of Medicine

English

Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability

American Journal of Human Genetics

English

Mutations in Linker for Activation of T Cells (LAT) Lead to a Novel Form of Severe Combined Immunodeficiency

Journal of Allergy and Clinical Immunology

English

Erratum To: Clinical and Molecular Aspects of Distal Renal Tubular Acidosis in Children

Pediatric Nephrology

English

Urea Is Successful in Treating Inappropriate Antidiuretic Hormone Secretion in an Infant

Acta Paediatrica, International Journal of Paediatrics

English

Crisponi Syndrome Is Caused by Mutations in the CRLF1 Gene and Is Allelic to Cold-Induced Sweating Syndrome Type 1

American Journal of Human Genetics

English

A Novel Missense Mutation (G43S) in the Switch I Region of Rab27A Causing Griscelli Syndrome

Molecular Genetics and Metabolism

Molecular Biology

English