Rapidly progressive spastic paraplegia due to hyperhomocysteinemia in child with MTHFR gene mutation and mitochondrial Complex I deficiency: A rare association-Reference-Cited by-同舟云学术

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Rapidly progressive spastic paraplegia due to hyperhomocysteinemia in child with MTHFR gene mutation and mitochondrial Complex I deficiency: A rare association

Published:2021 Issue:2 Volume:16 Page:153
ISSN:1817-1745
Container-title:Journal of Pediatric Neurosciences
language:en
Short-container-title:J Pediatr Neurosci

Author:

Mahale RohanR,Gautam Jyothi,Arunachal Gautam,Alappati Sandhya,Varghese Nibu,Kovoor Jennifer,Mailankody Pooja,Padmanabha Hansashree,Pavagada Mathuranath

Publisher

Medknow

Subject

General Neuroscience,Pediatrics, Perinatology and Child Health

Cited by 2 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

1. Evaluation of the clinical, biochemical, and genetic presentation of neonatal and adult-onset 5,10-methylene tetrahydrofolate reductase (MTHFR) deficiency in patients from Pakistan;Journal of Pediatric Endocrinology and Metabolism;2023-07-13

2. Adolescent/Adult-Onset Leukodystrophy with MTHFR Deficiency – A Treatable Cause;Neurology India;2023

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