Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report

Authors

Institutions

Publication Details

Journal
Current Journal of Neurology
Published
2024-09-09
DOI
https://doi.org/10.18502/cjn.v23i1.16439
Primary Topic
Erythrocyte Function and Pathophysiology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report

Shahriar Nafissi, Seyed Jalaleddin Hadei, Bardiya Ghaderi-Yazdi
Current Journal of Neurology
Erythrocyte Function and Pathophysiology
article

Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report

Shahriar Nafissi, Seyed Jalaleddin Hadei, Bardiya Ghaderi-Yazdi
article en

Abstract

No abstract available for this paper.
Current Journal of NeurologyVol. 23(1)
Shariati Hospital (IR), Tehran University of Medical Sciences (IR)
Openalex Percentile: Top 80%
Erythrocyte Function and Pathophysiology
DOIOpen Access PDFOpenAlex
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report — Shahriar Nafissi, Seyed Jalaleddin Hadei, et al. · Current Journal of Neurology (2024) | TGRS Research Map | TGRS