Cargando…
Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome”
| Autores principales: | , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Korean Movement Disorder Society
2021
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490183/ https://www.ncbi.nlm.nih.gov/pubmed/33819419 http://dx.doi.org/10.14802/jmd.20145 |
| _version_ | 1784578476335955968 |
|---|---|
| author | Walker, Ruth Helen Hegele, Robert Alexander Danek, Adrian |
| author_facet | Walker, Ruth Helen Hegele, Robert Alexander Danek, Adrian |
| author_sort | Walker, Ruth Helen |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-8490183 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2021 |
| publisher | The Korean Movement Disorder Society |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-84901832021-10-13 Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome” Walker, Ruth Helen Hegele, Robert Alexander Danek, Adrian J Mov Disord Letter to the Editor The Korean Movement Disorder Society 2021-09 2021-04-06 /pmc/articles/PMC8490183/ /pubmed/33819419 http://dx.doi.org/10.14802/jmd.20145 Text en Copyright © 2021 The Korean Movement Disorder Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Letter to the Editor Walker, Ruth Helen Hegele, Robert Alexander Danek, Adrian Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome” |
| title | Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome” |
| title_full | Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome” |
| title_fullStr | Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome” |
| title_full_unstemmed | Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome” |
| title_short | Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome” |
| title_sort | comment on “a new allelic variant in the pank2 gene in a patient with incomplete harp syndrome” |
| topic | Letter to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490183/ https://www.ncbi.nlm.nih.gov/pubmed/33819419 http://dx.doi.org/10.14802/jmd.20145 |
| work_keys_str_mv | AT walkerruthhelen commentonanewallelicvariantinthepank2geneinapatientwithincompleteharpsyndrome AT hegelerobertalexander commentonanewallelicvariantinthepank2geneinapatientwithincompleteharpsyndrome AT danekadrian commentonanewallelicvariantinthepank2geneinapatientwithincompleteharpsyndrome |