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6. and Weleber, Richard G RG. 2002-06 Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture). [PMID:12187427]
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8.Jacobi, Felix Karl FK and 7 more authors. 2003-05 A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness. [PMID:12719097]
9.Jalkanen, R R and 8 more authors. 2003-06 A new genetic locus for X linked progressive cone-rod dystrophy. [PMID:12807962]
10.Koschak, Alexandra A and 6 more authors. 2003-07-09 Cav1.4alpha1 subunits can form slowly inactivating dihydropyridine-sensitive L-type Ca2+ channels lacking Ca2+-dependent inactivation. [PMID:12853422]