Mutation in a short-chain collagen gene, CTRP5 , results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

By Hayward Caroline  

Human Molecular Genetics, Vol. 12, Iss. 20, 2003-10 ,pp. : 2657-2667

Oxford University Press

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A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration

By Chavali Venkata R.M.   Khan Naheed W.   Cukras Catherine A.   Bartsch Dirk-Uwe   Jablonski Monica M.   Ayyagari Radha  

Human Molecular Genetics, Vol. 20, Iss. 10, 2011-05 ,pp. : 2000-2014

Oxford University Press

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Analysis of the ARMD1 locus: evidence that a mutation in HEMICENTIN-1 is associated with age-related macular degeneration in a large family

By Schultz Dennis W.  

Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3315-3323

Oxford University Press

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A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration

By Maw Marion A.   Corbeil Denis  

Human Molecular Genetics, Vol. 9, Iss. 1, 2000-01 ,pp. : 27-34

Oxford University Press

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Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease

By Li Yonghong   Grupe Andrew   Rowland Charles   Holmans Peter   Segurado Ricardo   Abraham Richard   Jones Lesley   Catanese Joseph   Ross David   Mayo Kevin   Martinez Maribel   Hollingworth Paul   Goate Alison   Cairns Nigel J.   Racette Brad A.   Perlmutter Joel S.   O'Donovan Michael C.   Morris John C.   Brayne Carol   Rubinsztein David C.   Lovestone Simon   Thal Leon J.   Owen Michael J.   Williams Julie  

Human Molecular Genetics, Vol. 17, Iss. 5, 2008-03 ,pp. : 759-767

Oxford University Press

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