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Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during Infancy.

Journal: American Journal of Human Genetics

Published: 2019-09-27

DOI: 10.1016/j.ajhg.2019.09.011

Affiliations: 23

Authors: 22

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Institutions Share
Beijing Key Laboratory of Molecular Diagnosis and Study on Pediatric Genetic Diseases, Peking University First Hospital, China 0.14
Amsterdam Neuroscience, Netherlands 0.10
Institute for Molecular Bioscience (IMB), UQ, Australia 0.09
Molecular and Behavioral Neuroscience Institute (MBNI), U-M, United States of America (USA) 0.07
Dorris Neuroscience Center (DNC), Scripps Research, United States of America (USA) 0.07
Department of Neuroscience, Scripps Research, United States of America (USA) 0.07
CSIRO Data61, Australia 0.05
Peking University First Hospital, China 0.05
Illumina, Inc., United States of America (USA) 0.05
Murdoch Childrens Research Institute (MCRI), Australia 0.05
MOE Laboratory of Neuroscience, PUHSC PKU, China 0.04
Department of Clinical Chemistry, VUmc, Netherlands 0.03
Amsterdam Gastroenterology and Metabolism, UvA, Netherlands 0.03
Joint International Research Center of Translational and Clinical Research, PKU, China 0.03
UMC Utrecht Brain Center Rudolf Magnus, Netherlands 0.02
Children's Hospital, ZJU, China 0.02
Henan Provincial Key Laboratory of Children's Genetic and Metabolic Diseases at Children's Hospital, ZZU, China 0.02
Wilhelmina Children's Hospital, Netherlands 0.02
Laboratory Genetic Metabolic Diseases (LGMD), UvA, Netherlands 0.01
Department of Psychiatry, U-M, United States of America (USA) 0.01
Department of Human Genetics, U-M, United States of America (USA) 0.01
Department of Computational Medicine and Bioinformatics (DCM&B), U-M, United States of America (USA) 0.01

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