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FOXRED1 silencing in mice: A possible animal model for Leigh Syndrome

Genetic-environment interactions in a case-control study of Parkinson’s Disease in Egypt

Migration Gender and Social Inclusion

siRNA blocking of mammalian target of rapamycin

UCHL3 regulates topoisomerase induced chromosomal break repair

Possible targets for diagnosis of Parkinson’s and Alzheimer’s diseases

Implementing safeguarding and personalisation in social work

Novel mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia

Possible therapy for tauopathy in cellular model

C9orf72 expansion disrupts ATM-mediated chromosomal break repair

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