文献
J-GLOBAL ID:201202201153291996
整理番号:12A1218986
PTCH1蛋白質の長いアイソフォームの選択的ハプロ不全は母斑性基底細胞癌症候群を引き起こせる
Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome
著者 (10件):
SUZUKI Maiko
(Kitasato Univ. Graduate School of Medical Sci., Sagamihara, JPN)
,
HATSUSE Hiromi
(Kitasato Univ. Graduate School of Medical Sci., Sagamihara, JPN)
,
NAGAO Kazuaki
(Kitasato Univ. Graduate School of Medical Sci., Sagamihara, JPN)
,
TAKAYAMA Yoshinaga
(Kitasato Univ. Graduate School of Medical Sci., Sagamihara, JPN)
,
KAMEYAMA Kohzoh
(Kitasato Univ. Graduate School of Medical Sci., Sagamihara, JPN)
,
KABASAWA Yuji
(Tokyo Medical and Dental Univ., Tokyo, JPN)
,
OMURA Ken
(Tokyo Medical and Dental Univ., Tokyo, JPN)
,
YOSHIDA Masayuki
(Tokyo Medical and Dental Univ., Tokyo, JPN)
,
FUJII Katsunori
(Chiba Univ. Graduate School of Medicine, Chiba, JPN)
,
MIYASHITA Toshiyuki
(Kitasato Univ. Graduate School of Medical Sci., Sagamihara, JPN)
資料名:
Journal of Human Genetics
(Journal of Human Genetics)
巻:
57
号:
7
ページ:
422-426
発行年:
2012年07月
JST資料番号:
Z0756A
ISSN:
1434-5161
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
イギリス (GBR)
言語:
英語 (EN)