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A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666852/ https://www.ncbi.nlm.nih.gov/pubmed/38022434 http://dx.doi.org/10.4103/aian.aian_428_23 |
| _version_ | 1785139131098071040 |
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| author | Prabhu, Sameeta M. Banerjee, Bidisha Shetty, Mitesh |
| author_facet | Prabhu, Sameeta M. Banerjee, Bidisha Shetty, Mitesh |
| author_sort | Prabhu, Sameeta M. |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-10666852 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | Wolters Kluwer - Medknow |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-106668522023-09-01 A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India Prabhu, Sameeta M. Banerjee, Bidisha Shetty, Mitesh Ann Indian Acad Neurol Letters to the Editor Wolters Kluwer - Medknow 2023 2023-10-13 /pmc/articles/PMC10666852/ /pubmed/38022434 http://dx.doi.org/10.4103/aian.aian_428_23 Text en Copyright: © 2023 Annals of Indian Academy of Neurology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
| spellingShingle | Letters to the Editor Prabhu, Sameeta M. Banerjee, Bidisha Shetty, Mitesh A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India |
| title | A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India |
| title_full | A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India |
| title_fullStr | A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India |
| title_full_unstemmed | A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India |
| title_short | A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India |
| title_sort | novel pgk1 gene variant with neurological dysfunction, haemolytic anaemia and myopathy: a case report from india |
| topic | Letters to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666852/ https://www.ncbi.nlm.nih.gov/pubmed/38022434 http://dx.doi.org/10.4103/aian.aian_428_23 |
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