Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3

By Sidjanin D.J.  

Human Molecular Genetics, Vol. 11, Iss. 16, 2002-08 ,pp. : 1823-1833

Oxford University Press

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Mutations in the CNGB3 gene encoding the β -subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia ( ACHM3 ) linked to chromosome 8q21

By Kohl Susanne  

Human Molecular Genetics, Vol. 9, Iss. 14, 2000-09 ,pp. : 2107-2116

Oxford University Press

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Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice

By Haider N.B.   Naggert J.   Nishina P.M.  

Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1619-1626

Oxford University Press

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Caveolin-3 deficiency causes muscle degeneration in mice

By Hagiwara Yasuko   Sasaoka Toshikuni   Araishi Kenji   Imamura Michihiro   Yorifuji Hiroshi   Nonaka Ikuya   Ozawa Eijiro   Kikuchi Tateki  

Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3047-3054

Oxford University Press

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Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity

By Haider Neena  

Mammalian Genome, Vol. 19, Iss. 3, 2008-03 ,pp. : 145-154

Springer Publishing Company

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