文献
J-GLOBAL ID:201502211109793524
整理番号:15A1167694
母系-遺伝のERCC8の全遺伝子欠失と父系-遺伝のERCC8エキソン4欠失によるコケイン症候群
Cockayne Syndrome due to a maternally-inherited whole gene deletion of ERCC8 and a paternally-inherited ERCC8 exon 4 deletion
著者 (11件):
TING T.W.
(KK Women’s and Children’s Hospital, Singapore)
,
BRETT M.S.
(KK Women’s and Children’s Hospital, Singapore)
,
TAN E.S.
(KK Women’s and Children’s Hospital, Singapore)
,
SHEN Y.
(Children’s Hospital, Boston, USA)
,
LEE S.P.
(KK Women’s and Children’s Hospital, Singapore)
,
LIM E.C.
(KK Women’s and Children’s Hospital, Singapore)
,
VASANWALA R.F.
(KK Women’s and Children’s Hospital, Singapore)
,
LEK N.
(KK Women’s and Children’s Hospital, Singapore)
,
THOMAS T.
(KK Women’s and Children’s Hospital, Singapore)
,
LIM K.W.
(KK Women’s and Children’s Hospital, Singapore)
,
TAN E.C.
(KK Women’s and Children’s Hospital, Singapore)
資料名:
Gene
(Gene)
巻:
572
号:
2
ページ:
274-278
発行年:
2015年11月10日
JST資料番号:
E0701B
ISSN:
0378-1119
資料種別:
逐次刊行物 (A)
記事区分:
短報
発行国:
オランダ (NLD)
言語:
英語 (EN)