novel phenotype-genotype correlation with PEX6 gene in Saudi patients with heimler syndrome

被引：0
|
作者：
Almoallem, Basamat [1 ]
机构：
[1] King Saud Univ, Dept Ophthalmol, Riyadh, Saudi Arabia
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2022年 / 30卷 / SUPPL 1期
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：
P02.054.C
引用
收藏
页码：134 / 135
页数：2
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