Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage

The modification of genes in animal models has evidently and comprehensively improved our knowledge on proteins and signaling pathways in human physiology and pathology. In this review, we discuss almost 40 monogenic rare diseases that are enriched in the Finnish population and defined as the Finnis...

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Detalles Bibliográficos
Autores principales: Zárybnický, Tomáš, Heikkinen, Anne, Kangas, Salla M., Karikoski, Marika, Martínez-Nieto, Guillermo Antonio, Salo, Miia H., Uusimaa, Johanna, Vuolteenaho, Reetta, Hinttala, Reetta, Sipilä, Petra, Kuure, Satu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621025/
https://www.ncbi.nlm.nih.gov/pubmed/34831381
http://dx.doi.org/10.3390/cells10113158

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621025/
https://www.ncbi.nlm.nih.gov/pubmed/34831381
http://dx.doi.org/10.3390/cells10113158

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