Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by a novel MFF gene mutation in a young child-Reference-Cited by-同舟云学术

Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by a novel MFF gene mutation in a young child

Author:

Panda Isha¹,Ahmad Istaq²,Sagar Shakti³⁴,Zahra Sana²,Shamim Uzma²,Sharma Suvasini¹,Faruq Mohammed²⁴^ORCID

Affiliation:

1. Neurology Division, Department of PediatricsLady Hardinge Medical College and Associated Kalawati Saran Children's Hospital New Delhi India

2. Genomics and Molecular MedicineCSIR‐Institute of Genomics and Integrative Biology Delhi India

3. Centre of Excellence for Translational Research in Asthma and Lung DiseasesCSIR‐Institute of Genomics and Integrative Biology New Delhi India

4. Academy of Scientific and Innovative Research (AcSIR) India

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference6 articles.

3. Clinical and biochemical features in a patient with mitochondrial fission factor gene alteration;Nasca A;Front Genet,2018

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献