De novo KCNH1 mutations in four patients with syndromic developmental delay, hypotonia and seizures

• Ryoko Fukai

• Hirotomo Saitsu

• Yoshinori Tsurusaki

• Yasunari Sakai

• Kazuhiro Haginoya

• Kazumasa Takahashi

• Monika Weisz Hubshman

• Nobuhiko Okamoto

• Mitsuko Nakashima

• Fumiaki Tanaka

• Noriko Miyake

• Naomichi Matsumoto

Journal

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 61 (5), 381-387, 2016-05

  Tokyo : Springer Nature

Details

• CRID: 1521136280409491072
• NII Article ID: 40020825171
• NII Book ID: AA11206160
• ISSN: 14345161
• NDL BIB ID: 027303405
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I027303405
• Web Site: https://search.jamas.or.jp/link/ui/2017020894
• Text Lang: en
• NDL Source Classification:
  • ZS16(科学技術--医学--人類遺伝学)
• Data Source:
  • NDL
  • CiNii Articles