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Autosomal recessive retinitis pigmentosa of the molecular genetics of

249 passwords in the event of rG-T of the base substitution (Glu249stupj. which led to nonsense mutations. encoding a significant shortening and no functional rhodopsin protein,[link widoczny dla zalogowanych], visual disturbance caused by the rhodopsin gene in this paper, the fifth exon Untranslated in the field of high- frequency DNA polymorphisms, elm test in which inbreeding family, the eyes are normal parents A / G heterozygotes. and the sick for the G / G net table . so do not rule out the family and as Rhodopsin genes have been used as the detection Liu as the other inbreeding ARRP family ,[link widoczny dla zalogowanych], family members of the umbrella department for the A / G heterozygotes (Figure I】 , thus Practical instigate Medicine Volume 20 {2002J No. 2 to Exclude the family and rhodopsin genes : Maw other reports of autosomal recessive disease of small mouth ,[link widoczny dla zalogowanych], which is the use of DNA polymorphism and its disease-related detection of an example of the abnormal gene . For this study Test results. ARRP family and the rhodopsin gene mutation in coding region of the irrelevant ,[link widoczny dla zalogowanych], if the RP was detected in other candidate genes may be able to find out the cause of diseases associated with mutations
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