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2001 | 1 |
2006 | 1 |
2024 | 0 |
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Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy.
Acta Ophthalmol Scand. 2001 Aug;79(4):359-65. doi: 10.1034/j.1600-0420.2001.079004359.x.
Acta Ophthalmol Scand. 2001.
PMID: 11453854
Free article.
X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
Jalkanen R, Mäntyjärvi M, Tobias R, Isosomppi J, Sankila EM, Alitalo T, Bech-Hansen NT.
Jalkanen R, et al.
J Med Genet. 2006 Aug;43(8):699-704. doi: 10.1136/jmg.2006.040741. Epub 2006 Feb 27.
J Med Genet. 2006.
PMID: 16505158
Free PMC article.
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