Evidence map›Paper›PMID 41994224›Full record

ArticleNeurology. Genetics2026

Novel

Ke Xu, Sen Zeng, Xiaobo Li, Zhongzheng Li, Yue Liu, Mengli Wang, Yongzhi Xie, Lei Liu, Wanqian Cao, Shunxiang Huang and 3 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Neurology. Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Ke XuDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0000-0001-9114-1535
Sen ZengDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0000-0002-5458-8474
Xiaobo LiDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0009-0007-1241-4015
Zhongzheng LiDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0009-0000-4718-1361
Yue LiuDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0009-0002-5840-7789
Mengli WangDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0009-0009-2567-382X
Yongzhi XieDepartment of Radiology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0000-0003-4212-9737
Lei LiuHealth Management Center, the Third Xiangya Hospital, Central South University, Changsha, China; and.ORCID https://orcid.org/0000-0002-3448-4264
Wanqian CaoDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0000-0001-5546-9402
Shunxiang HuangDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0009-0009-2281-8560
Huadong ZhaoDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0009-0005-7656-6750
Beisha TangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0000-0003-2120-1576
Ruxu ZhangDepartment of Neurology, the Third Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0000-0003-3823-8148

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Biallelic Methods: Eight families were identified from a cohort of 351 families with axonal CMTR, including axonal CMT and distal hereditary motor neuropathies (dHMN). Clinical and genetic data were retrospectively analyzed. Haplotype analysis investigated the founder effect of the high-frequency variant, and RNA sequencing was conducted for the splice variant. A systematic literature review (PubMed/CNKI, 2009-2025) was performed to compile global cases. Results: Discussion: This study identifies 8 novel

Identifiers

PMID41994224
PMCPMC13082243

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.