A new genetic locus for X linked progressive cone-rod dystrophy. (Original Articles)

Authors :: Jalkanen, R.
Demirci, F.Y.
Tyynismaa, H.
Bech-Hansen, T.
Meindl, A.
Peippo, M.
Mantyjarvi, M.
Gorin, M.B.
Alitalo, T.
Source :: Journal of Medical Genetics. June 2003, Vol. 40 Issue 6, p418, 6 p.
Publication Year :: 2003
Abstract: X linked progressive cone-rod dystrophy (COD) is a retinal disease primarily affecting the cone photoreceptors. The disease is genetically heterogeneous and two loci, COD 1 (Xp21.1-11.4) and COD2 (Xq27.2-28), have [...]

Subjects :: Retinal diseases -- Genetic aspects
X chromosome -- Abnormalities -- Genetic aspects
Cones (Photoreceptors) -- Abnormalities -- Genetic aspects
Health
Genetic aspects
Abnormalities

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