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Transgenic LRRK2(R1441G) rats–a model for Parkinson disease?

Parkinson disease (PD) is the most common movement disorder, characterized by the progressive degeneration of dopaminergic neurons in the substantia nigra. While the cause of this disease is largely unknown, a rare autosomal dominant familial form of PD is caused by a genetic mutation in the leucine...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:PeerJ
Egile Nagusiak: Shaikh, Komal T., Yang, Alvin, Youshin, Ekaterina, Schmid, Susanne
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: PeerJ Inc. 2015
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4435452/
https://ncbi.nlm.nih.gov/pubmed/26020005
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.945
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