ArticleFrontiers in neurology2022
Case report: Unusual episodic myopathy in a patient with novel homozygous deletion of first coding exon of
Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed, 5 citations in OpenAlex.
- MICU1 myopathy revisited: phenotypic variability in a rare mitochondrial calcium disorder.Acta neurologica Belgica · 2025Article
- MICU1 related myopathy - a rare report from India.Journal of neuromuscular diseases · 2024Article
- Dolichocephaly, Arachnodactyly, Diplopia, and Distal Myopathy - Novel Phenotype of MICU1 Variant c.553C>T.Cureus · 2024Article
- Autosomal Recessive Mitochondrial Myopathy due to MICU-1 Variants.Annals of Indian Academy of NeurologyArticle
Corrections and comments
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Authors and funding
9 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We present a patient with unusual episodes of muscular weakness due to homozygous deletion of exon 2 in the
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.