Oliver-McFarlane syndrome: mutations of PNPLA6 and follow-up of 30 years in two brothers

被引：0
|
作者：
Jedraszak, G. [1 ]
de Roux, N. [2 ]
Jobic, F.
Desailloud, R. [3 ]
Bony, H.
Milazzo, S. [4 ]
Mathieu-Dramard, M.
Morin, G.
机构：
[1] Lab Human Genet, Amiens, France
[2] Hop Robert Debre, Lab Biochim Hormonol, Paris, France
[3] Serv Endocrinol, Amiens, France
[4] Serv Ophthalmol, Amiens, France
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P11.068D
引用
收藏
页码：373 / 373
页数：1
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