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Autosomal recessive retinitis pigmentosa mutations of disease genes PDE6B

Related to the family because of ARRP disease usually small number of multi-form of the distribution,[link widoczny dla zalogowanych], and sporadic RP RP is the most common type. May also occur with our failure to detect exon mutations outside the area,[link widoczny dla zalogowanych], such as the 3 UTR intron control region and most of the area concerned. Of course not rule out the Chinese population is different from the genetic pool in Europe,[link widoczny dla zalogowanych], PDE6B genes are not the main Chinese ARRP disease genes.
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