Volume number61(5):2016.5
De novo KC...

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

Icons representing 記事

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

Call No. (NDL)
Z54-H248
Bibliographic ID of National Diet Library
027303405
Material type
記事
Author
Ryoko Fukaiほか
Publisher
Tokyo : Springer Nature
Publication date
2016-05
Material Format
Paper
Journal name
Journal of human genetics / Japan Society of Human Genetics 61(5):2016.5
Publication Page
p.381-387
View All

Holdings of Libraries in Japan

This page shows libraries in Japan other than the National Diet Library that hold the material.

Please contact your local library for information on how to use materials or whether it is possible to request materials from the holding libraries.

other

  • CiNii Research

    Search Service
    You can check the holdings of institutions and databases with which CiNii Research is linked at the site of CiNii Research.

Bibliographic Record

You can check the details of this material, its authority (keywords that refer to materials on the same subject, author's name, etc.), etc.

Paper

Material Type
記事
Author/Editor
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
Periodical title
Journal of human genetics / Japan Society of Human Genetics
No. or year of volume/issue
61(5):2016.5
Volume
61
Issue
5
Pages
381-387
Publication date of volume/issue (W3CDTF)
2016-05