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Jervell and Lange-Nielsen syndrome with novel KCNQ1 and additional gene mutations.
Matsuda, Shinichi; Ohnuki, Yuko; Okami, Mayuri; Ochiai, Eriko; Yamada, Shiro; Takahashi, Kazumi; Osawa, Motoki; Okami, Kenji; Iida, Masahiro; Mochizuki, Hiroyuki.
Affiliation
  • Matsuda S; Department of Pediatrics, Tokai University School of Medicine, Isehara, Japan.
  • Ohnuki Y; Department of Medical Ethics, Tokai University School of Medicine, Isehara, Japan.
  • Okami M; Department of Clinical Genetics, Tokai University Hospital, Isehara, Japan.
  • Ochiai E; Department of Clinical Genetics, Tokai University Hospital, Isehara, Japan.
  • Yamada S; Department of Otolaryngology, Tokai University School of Medicine, Isehara, Japan.
  • Takahashi K; Department of Otolaryngology, Samukawa Hospital, Samukawa, Japan.
  • Osawa M; Department of Forensic Medicine, Tokai University School of Medicine, Isehara, Japan.
  • Okami K; Department of Pediatrics, Tokai University Oiso Hospital, Oiso, Japan.
  • Iida M; Department of Medical Ethics, Tokai University School of Medicine, Isehara, Japan.
  • Mochizuki H; Department of Clinical Genetics, Tokai University Hospital, Isehara, Japan.
Hum Genome Var ; 7: 34, 2020.
Article in En | MEDLINE | ID: mdl-33082985
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Hum Genome Var Year: 2020 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Hum Genome Var Year: 2020 Document type: Article Affiliation country: Country of publication: