| Title | Authors | Year | Journal |
|---|---|---|---|
| Clinical and molecular features of mitochondrial DNA depletion syndromes. | Invernizzi F | 2009 | Journal of inherited metabolic disease |
| Two novel POLG1 mutations in a patient with progressive external ophthalmoplegia, levodopa-responsive pseudo-orthostatic tremor and parkinsonism. | Invernizzi F | 2008 | Neuromuscular disorders : NMD |
Version:20250305
This page provides a summary of the entries in Polbase associated with this author.
The publication history graph presents the number of publications in Polbase by this author over time.
The polymerase chart indicates which polymerases this author has published on.
Polbase automatically discovers many polymerase papers as they are published. Some relevant papers are not included because the algorithm is designed to reduce background. Please contribute to polbase by adding your missing DNA polymerase papers.
The symbol in the upper-right corner of the page
links to this help text. The question mark icon is used everywhere to indicate that help is available.
Tables may be sorted by clicking on any of the column titles. A second click reverses the sort order. <Ctrl> + click on the column titles to sort by more than one column (e.g. family then name).
Filtering:It is also possible to filter the table by typing into the search box above the table. This will instantly hide lines from the table that do not contain your search text.