Rare Heterozygous Loss‐of‐Function Variants in <scp> <i>MCOLN1</i> </scp> Identified in Two Sporadic Patients with <scp>α</scp> ‐Synucleinopathies

Chenxin Ying, Xinhui Chen, Zhidong Cen, Xinghua Feng, Nan Jin, Jiaxiang Li, Xinchen Wang, Wei Luo

Open source

DOI: 10.1002/mds.70469
Published: 2026-08-05
Container: Movement Disorders
Publisher: Wiley
Open access: unknown

Credibility signals

uncertain Score 64/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

supportingDOI registered: A matching record was returned by Crossref. Source: Crossref; license: CC0 metadata
supportingDOI resolves: A matching record was returned by Crossref. Source: Crossref; license: CC0 metadata
not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility. Source: DOAJ; license: CC0
not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredROR affiliation: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredOpen access status: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredPublication license: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredPublication version: A publication version was supplied but is not scored. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
supportingMetadata completeness: All 6 scored descriptive metadata groups are present. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer

Cite this work

BibTeX

@article{allodium:10.1002/mds.70469,
  title = {Rare Heterozygous Loss‐of‐Function Variants in
                    <scp>
                      <i>MCOLN1</i>
                    </scp>
                    Identified in Two Sporadic Patients with
                    <scp>α</scp>
                    ‐Synucleinopathies},
  author = {Chenxin Ying and Xinhui Chen and Zhidong Cen and Xinghua Feng and Nan Jin and Jiaxiang Li and Xinchen Wang and Wei Luo},
  year = {2026},
  journal = {Movement Disorders},
  doi = {10.1002/mds.70469},
  url = {https://doi.org/10.1002/mds.70469}
}

RIS

TY  - JOUR
TI  - Rare Heterozygous Loss‐of‐Function Variants in
                    <scp>
                      <i>MCOLN1</i>
                    </scp>
                    Identified in Two Sporadic Patients with
                    <scp>α</scp>
                    ‐Synucleinopathies
AU  - Chenxin Ying
AU  - Xinhui Chen
AU  - Zhidong Cen
AU  - Xinghua Feng
AU  - Nan Jin
AU  - Jiaxiang Li
AU  - Xinchen Wang
AU  - Wei Luo
PY  - 2026
JO  - Movement Disorders
DO  - 10.1002/mds.70469
UR  - https://doi.org/10.1002/mds.70469
ER  -

APA

Ying, C., Chen, X., Cen, Z., Feng, X., Jin, N., Li, J., Wang, X., & Luo, W. (2026). Rare Heterozygous Loss‐of‐Function Variants in <scp> <i>MCOLN1</i> </scp> Identified in Two Sporadic Patients with <scp>α</scp> ‐Synucleinopathies. Movement Disorders. https://doi.org/10.1002/mds.70469

Source records

crossref · retrieved 2026-09-26T08:43:13.439Z