A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe

By Marconi R.  

Human Molecular Genetics, Vol. 8, Iss. 4, 1999-04 ,pp. : 567-574

Oxford University Press

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Functional association of the parkin gene promoter with idiopathic Parkinson's disease

By West A.B.  

Human Molecular Genetics, Vol. 11, Iss. 22, 2002-10 ,pp. : 2787-2792

Oxford University Press

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Leucine-rich repeat kinase 2 interacts with Parkin, DJ-1 and PINK-1 in a Drosophila melanogaster model of Parkinson's disease

By Venderova Katerina   Kabbach Ghassan   Abdel-Messih Elizabeth   Zhang Yi   Parks Robin J.   Imai Yuzuru   Gehrke Stephan   Ngsee Johnny   LaVoie Matthew J.   Slack Ruth S.   Rao Yong   Zhang Zhuohua   Lu Bingwei   Haque M. Emdadul   Park David S.  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4390-4404

Oxford University Press

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PKHDL1 , a homolog of the autosomal recessive polycystic kidney disease gene, encodes a receptor with inducible T lymphocyte expression

By Hogan M.C.   Griffin M.D.   Rossetti S.   Torres V.E.   Ward C.J.   Harris P.C.  

Human Molecular Genetics, Vol. 12, Iss. 6, 2003-03 ,pp. : 685-698

Oxford University Press

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Autosomal recessive retinitis pigmentosa and cone–rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

By Blankenagel A.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 355-362

Oxford University Press

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