bibliographic entry 5905001 [be/5905001]
https://w3id.org/oc/corpus/be/5905001

is a

• bibliographic reference

content

• Nichols, W. C, Pankratz, N, Hernandez, D, Paisan-Ruiz, C, Jain, S, Halter, C. A. (2005). Genetic screening for a single common LRRK2 mutation in familial Parkinson’s disease. Lancet 365 410–412. DOI: 10.1016/S0140-6736(05)17828-3 PMID: 15680455

references

• https://w3id.org/oc/corpus/br/5460