Clinico-Genetic Spectrum of POLG1 Mutation Carriers from India

被引：1
|
作者：
Finsterer, Josef [1 ]
机构：
[1] Messerli Inst, Klin Landstr, Vienna, Austria
来源：
JOURNAL OF MOLECULAR NEUROSCIENCE | 2022年 / 72卷 / 01期
关键词：
POLG1; Mitochondrial disorder; mtDNA; Phenotype; Heterogeneity; GENETICALLY CHARACTERIZED PATIENTS; MITOCHONDRIAL DISORDERS;
D O I：
10.1007/s12031-021-01905-8
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：
[No abstract available]
引用
收藏
页码：45 / 47
页数：3
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