Serum progranulin is not associated with rs5848 polymorphism in Korean patients with neurodegenerative diseases

Low serum progranulin (PGRN) is known to be associated with granulin (GRN) gene mutation and T alleles of GRN rs5848 polymorphism. However, there have been only a few Asian studies exploring these. We investigated the serum PGRN levels, rs5848 genotypes, and their relations with cerebrospinal fluid...

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Detalles Bibliográficos
Autores principales: Jung, Na-Yeon, Kim, Hyang-Sook, Kim, Eun Soo, Jeon, Sumin, Lee, Myung Jun, Pak, Kyoungjune, Lee, Jae-Hyeok, Lee, Young Min, Lee, Kangyoon, Shin, Jin-Hong, Ko, Jun Kyeung, Lee, Jae Meen, Yoon, Jin A., Hwang, Chungsu, Choi, Kyung-Un, Huh, Gi Yeong, Kim, Young-Eun, Kim, Eun-Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8794169/
https://www.ncbi.nlm.nih.gov/pubmed/35085262
http://dx.doi.org/10.1371/journal.pone.0261007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8794169/
https://www.ncbi.nlm.nih.gov/pubmed/35085262
http://dx.doi.org/10.1371/journal.pone.0261007

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