New type-4 D-bifunctional protein deficiency caused by compound heterozygous mutation of hydroxysteroid 17-beta dehydrogenase 4 (HSD17B4)

被引：0
|
作者：
McMillan, H. J.
Worthylake, T.
Geraghty, M.
Bulman, D.
Gottlieb, C.
Coupand, S.
Lawrence, S.
Boycott, K. M.
机构：
[1] Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada
[2] Ottawa Eye Inst, Ottawa, ON, Canada
来源：
JOURNAL OF NEUROLOGY | 2012年 / 259卷
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中图分类号：
R74 [神经病学与精神病学];
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页码：S43 / S43
页数：1
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