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Article

[Diagnosis of mitochondrial disorders in children with next generation sequencing].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Oct 2015

Liu Zhimei, Fang Fang, Ding Changhong, Zhang Weihua, Li Jiuwei, Yang Xinying, Wang Xiaohui, Wu Yun, Wang Hongmei, Liu Liying, Han Tongli, Wang Xu, Chen Chunhong, Lyu Junlan, Wu Husheng

Abstract excerpt

OBJECTIVE: To explore the application value of next generation sequencing (NGS) in the diagnosis of mitochondrial disorders. METHOD: According to mitochondrial disease criteria, genomic DNA was extracted using standard procedure from peripheral venous blood of patients with suspected mitochondrial disease collected from neurological department of Beijing Children's Hospital Affiliated to Capital Medical...

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Share to DNA, Mitochondrial
Share to High-Throughput Nucleotide Sequencing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Mitochondrial Encephalomyopathies

Share to Optic Atrophy, Hereditary, Leber

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Source

Identifiers

PMID: 26758110

Genes

CHAT
NDUFV1
PDHA1
SUCLA2
SUCLG1
SURF1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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