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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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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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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Association of the HTRA1 gene variant with age-related macular degeneration in the Japanese population

By Mori Keisuke   Horie-Inoue Kuniko   Kohda Masakazu   Kawasaki Izumi   Gehlbach Peter   Awata Takuya   Yoneya Shin   Okazaki Yasushi   Inoue Satoshi  

Journal of Human Genetics, Vol. 52, Iss. 7, 2007-07 ,pp. : 636-641

Springer Publishing Company

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