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Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996535/ https://www.ncbi.nlm.nih.gov/pubmed/36911455 http://dx.doi.org/10.4103/aian.aian_1118_21 |
| _version_ | 1784903065579552768 |
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| author | Kumar, Madhan Yoganathan, Sangeetha Todari, Siddarth Suresh, Parvathy Chandran, Mahalakshmi Danda, Sumita Mathew, Leni Grace Koshy, Beena Thomas, Maya |
| author_facet | Kumar, Madhan Yoganathan, Sangeetha Todari, Siddarth Suresh, Parvathy Chandran, Mahalakshmi Danda, Sumita Mathew, Leni Grace Koshy, Beena Thomas, Maya |
| author_sort | Kumar, Madhan |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-9996535 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2022 |
| publisher | Wolters Kluwer - Medknow |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-99965352023-03-10 Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations Kumar, Madhan Yoganathan, Sangeetha Todari, Siddarth Suresh, Parvathy Chandran, Mahalakshmi Danda, Sumita Mathew, Leni Grace Koshy, Beena Thomas, Maya Ann Indian Acad Neurol Letters to the Editor Wolters Kluwer - Medknow 2022 2022-12-03 /pmc/articles/PMC9996535/ /pubmed/36911455 http://dx.doi.org/10.4103/aian.aian_1118_21 Text en Copyright: © 2022 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 Kumar, Madhan Yoganathan, Sangeetha Todari, Siddarth Suresh, Parvathy Chandran, Mahalakshmi Danda, Sumita Mathew, Leni Grace Koshy, Beena Thomas, Maya Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations |
| title | Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations |
| title_full | Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations |
| title_fullStr | Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations |
| title_full_unstemmed | Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations |
| title_short | Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations |
| title_sort | hereditary folate malabsorption: a rare treatable disorder with hematological and neurological manifestations |
| topic | Letters to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996535/ https://www.ncbi.nlm.nih.gov/pubmed/36911455 http://dx.doi.org/10.4103/aian.aian_1118_21 |
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