Homozygous Deletion Related to Alu Repeats inRLBP1Causes Retinitis Punctata Albescens
Investigative Ophthalmology & Visual Science2006Vol. 47(11), pp. 4719–4719
Citations Over TimeTop 18% of 2006 papers
Ghyslaine Humbert, Cécile Delettre, Audrey Se ́ne ́chal, Ce ́cile Bazalgette, Abdelhamid Barakat, Christian Bazalgette, Bernard Arnaud, Guy Lenaers, Christian P. Hamel
Abstract
Because of the high density of Alu elements in RLBP1, a systematic search should be made for deletions in this gene when one or both alleles lack point mutations, in the case of RPA or flecked retinal dystrophy.
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