Author/Creator: Inaba, Mie - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Inaba, Mie

1. Biallelic loss of OTUD7A causes severe muscular hypotonia, intellectual disability, and seizures. Issue 4 (31st December 2020)

Authors:: Suzuki, Hisato; Inaba, Mie; Yamada, Mamiko; Uehara, Tomoko; Takenouchi, Toshiki; Mizuno, Seiji; Kosaki, Kenjiro; Doi, Motomichi
Journal:: American journal of medical genetics
Issue:: Volume 185:Issue 4(2021)
Page Start:: 1182
Record Type:: Journal Article
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2. Biallelic mutations in NALCN: Expanding the genotypic and phenotypic spectra of IHPRF1. Issue 2 (23rd November 2017)

Authors:: Takenouchi, Toshiki; Inaba, Mie; Uehara, Tomoko; Takahashi, Takao; Kosaki, Kenjiro; Mizuno, Seiji
Journal:: American journal of medical genetics
Issue:: Volume 176:Issue 2(2018)
Page Start:: 431
Record Type:: Journal Article
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3. R3HDM1 haploinsufficiency is associated with mild intellectual disability. Issue 6 (22nd March 2021)

Authors:: Fukushi, Daisuke; Inaba, Mie; Katoh, Kimiko; Suzuki, Yasuyo; Enokido, Yasushi; Nomura, Noriko; Tokita, Yoshihito; Hayashi, Shin; Mizuno, Seiji; Yamada, Kenichiro; Wakamatsu, Nobuaki
Journal:: American journal of medical genetics
Issue:: Volume 185:Issue 6(2021)
Page Start:: 1776
Record Type:: Journal Article
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