文献
J-GLOBAL ID:200902108653217606
整理番号:96A0651539
Two novel gene mutations (Glu174→Lys, Phe383→Tyr) causing the “hepatic” form of carnitine palmitoyltransferase II deficiency.
著者 (9件):
YAMAMOTO S
(Chiba Univ. School of Medicine, Chiba, JPN)
,
OHTAKE A
(Tokyo Metropolitan Inst. Medical Sci., Tokyo, JPN)
,
HAYASHIBE H
(Tokyo Metropolitan Inst. Medical Sci., Tokyo, JPN)
,
SAKURABA H
(Tokyo Metropolitan Inst. Medical Sci., Tokyo, JPN)
,
SUZUKI Y
(Tokyo Metropolitan Inst. Medical Sci., Tokyo, JPN)
,
ARAMAKI S
(Kurume Univ. School of Medicine, Kurume, JPN)
,
TAKAYANAGI M
(Chiba Children’s Hospital, Chiba, JPN)
,
HASEGAWA S
(Chiba City Inst. Health and Environment, Chiba, JPN)
,
NIIMI H
(Chiba Univ. School of Medicine, Chiba, JPN)
資料名:
Human Genetics
(Human Genetics)
巻:
98
号:
1
ページ:
116-118
発行年:
1996年07月
JST資料番号:
E0781B
ISSN:
0340-6717
CODEN:
HUGEDQ
資料種別:
逐次刊行物 (A)
発行国:
ドイツ (DEU)
言語:
英語 (EN)