Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II

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題名:	Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II
作者:	Chen, CP;Lin, SP;Tzen, CY;Tsai, FJ;Hwu, WL;Wan, WS
貢獻者:	附設醫院基因醫學部 Makay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan;Makay Mem Hosp, Dept Med Res, Taipei, Taiwan;Natl Yang Ming Univ, Dept Nursing, Taipei 112, Taiwan;Makay Mem Hosp, Dept Pediat, Taipei, Taiwan;Makay Mem Hosp, Dept Pathol, Taipei, Taiwan;China Med Univ Hosp, Dept Med Genet, Taichung, Taiwan;China Med Univ Hosp, Dept Pediat, Taichung, Taiwan;China Med Univ, Coll Chinese Med, Taichung, Taiwan;Natl Taiwan Univ Hosp, Dept Med Genet, Taipei, Taiwan;Natl Taiwan Univ Hosp, Dept Pediat, Taipei 10016, Taiwan
日期:	2004
上傳時間:	2010-09-20 13:57:07 (UTC+8)
出版者:	JOHN WILEY & SONS LTD
關聯:	PRENATAL DIAGNOSIS 24(3):230-232
顯示於類別:	[台中附設醫院] 會議論文

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