LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact

Detalles Bibliográficos
Autores principales: Beetz, Christian, Westenberger, Ana, Al‐Ali, Ruslan, Ameziane, Najim, Alhashmi, Nadia, Boustany, Rose‐Mary, Al Mutairi, Fuad, Alfadhel, Majid, Al‐Hassnan, Zuhair, AlSayed, Moenaldeen, Kandaswamy, Krishna K., Paknia, Omid, Skrahina, Volha, Rolfs, Arndt, Bauer, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Regular Issue Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248088/
https://www.ncbi.nlm.nih.gov/pubmed/33433017
http://dx.doi.org/10.1002/mds.28452

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248088/
https://www.ncbi.nlm.nih.gov/pubmed/33433017
http://dx.doi.org/10.1002/mds.28452

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