Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors
Sarah J. Pickett, John P. Grady, Yi Shiau Ng, Gráinne S. Gorman, Andrew M. Schaefer, Ian Wilson, Heather Jane Cordell, Douglass M. Turnbull, Robert William Taylor, Robert McFarland
- ISSN / E-ISSN
- — / —
- DOI
- 10.1002/acn3.532 ↗
- Volume · Issue · Pages
- 5 · 3 · 333-345
- Publisher
- John Wiley & Sons Inc.
- Article URL
- https://doi.org/10.1002/acn3.532 ↗
- Article details
- Unverified
Publication date (each date has its type and source)
07 Feb 2018
OpenAlex publication date · source: OpenAlex
| Type | Date | Source |
|---|---|---|
| OpenAlex publication date | 07 Feb 2018 | OpenAlex |
Keywords (as given): m.3243A>G mutation; mitochondrial disease; phenotypic heterogeneity; heritability; hearing loss; stroke-like episodes; seizures; ataxia; cognitive impairment; migraine; asymptomatic carriers; prognosis
HEC Status at Publication Not the journal's current status
HEC Status at PublicationNot conclusive
Historical status could not be conclusively determined.
- HEC status cannot be determined for this date: no HEC list is recorded as in effect on it.
Best available information, not a definitive status: HEC status cannot be determined for this date: no HEC list is recorded as in effect on it.
- Journal
- Annals of Clinical and Translational Neurology
- Publication date used
- 07 Feb 2018 (OpenAlex publication date)
- Applicable HEC period
- None recorded for this date
- Category
- —
- Recognition status
- Unknown (NO_PERIOD_FOR_DATE)
- Source
- —
- Verification status
- Not available
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