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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: May 27, 2023. (Total: 217315Documents)
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Query Trace: Ankyrin-b Syndrome[original query]
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes.
Circulation journal : official journal of the Japanese Circulation Society 2016 Oct .
Ichikawa Mari, Aiba Takeshi, Ohno Seiko, Shigemizu Daichi, Ozawa Junichi, Sonoda Keiko, Fukuyama Megumi, Itoh Hideki, Miyamoto Yoshihiro, Tsunoda Tatsuhiko, Makiyama Takeru, Tanaka Toshihiro, Shimizu Wataru, Horie Mino
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