Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica.

Kim J, Hahn Y, Sohn EH, Lee YJ, Yun JH, Kim JM, Chung JH

DOI: 10.1136/jnnp.70.5.618
Published: 2001 May
Container: Journal of neurology, neurosurgery, and psychiatry
Publisher: Not recorded
Open access: yes

Credibility signals

limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

cautionDOI registered: No matching Crossref record was present in this response. Source: Crossref; license: CC0 metadata
cautionDOI resolves: No matching Crossref record was present in this response. 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
supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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
cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer

Cite this work

BibTeX

@article{allodium:10.1136/jnnp.70.5.618,
  title = {Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica.},
  author = {Kim J and Hahn Y and Sohn EH and Lee YJ and Yun JH and Kim JM and Chung JH},
  year = {2001},
  journal = {Journal of neurology, neurosurgery, and psychiatry},
  doi = {10.1136/jnnp.70.5.618},
  url = {https://doi.org/10.1136/jnnp.70.5.618}
}

RIS

TY  - JOUR
TI  - Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica.
AU  - Kim J
AU  - Hahn Y
AU  - Sohn EH
AU  - Lee YJ
AU  - Yun JH
AU  - Kim JM
AU  - Chung JH
PY  - 2001
JO  - Journal of neurology, neurosurgery, and psychiatry
DO  - 10.1136/jnnp.70.5.618
UR  - https://doi.org/10.1136/jnnp.70.5.618
ER  -

APA

J, K., Y, H., EH, S., YJ, L., JH, Y., JM, K., & JH, C. (2001). Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica.. Journal of neurology, neurosurgery, and psychiatry. https://doi.org/10.1136/jnnp.70.5.618

Source records

pubmed · retrieved 2026-09-25T16:42:09.329Z