The case of Hutchinson-Gildford Syndrome associated with G608G mutation in LMNA gene and Methylenetetrahydrofolate reductase deficiency

被引：0
|
作者：
Hrechanina, Y. [1 ]
Molodan, L. [1 ]
机构：
[1] Kharkiv Natl Med Univ, Interreg Specialized Med Genet Ctr, Ctr Rare Orphan Dis, Kharkiv, Ukraine
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2020年 / 28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：
E-P12.37
引用
收藏
页码：939 / 939
页数：1
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