Shogo Furukawa
4PUBLICATIONS
8CO-AUTHORS
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Publications (4)
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|Jan 06, 2026
Identification of 5' untranslated region variants in genes involved in neurodevelopmental disorders.Taiju Hayashi, Sachiko Miyamoto, Yusaku Endo
|Aug 09, 2024
Exploring unsolved cases of lissencephaly spectrum: integrating exome and genome sequencing for higher diagnostic yield.Shogo Furukawa, Mitsuhiro Kato, Akihiko Ishiyama
|Oct 23, 2023
Novel compound heterozygous ATP1A2 variants in a patient with fetal akinesia/hypokinesia sequence.Shogo Furukawa, Mitsuhiro Kato, Toshihiro Nomura
|Feb 19, 2022
Two novel heterozygous variants in ATP1A3 cause movement disorders.Shogo Furukawa, Sachiko Miyamoto, Shinobu Fukumura
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