Corrigendum: Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa
نویسندگان
چکیده
In Table 1, for Family RP-1929 the nucleotide change 'c.9079dupA' and protein change 'p.Arg3027Lysfs*9' were incorrectly given as 'c.9142dupA' and 'p.Arg3048Lysfs*9' respectively. In Table 2, for Family RP-1147 the cDNA 'c.830G > A' and protein 'p.Arg277Gln' were incorrectly given as 'c.1037G > A' and 'p.Arg346Gln' respectively. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit
منابع مشابه
Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa
Retinitis pigmentosa (RP) is a group of inherited progressive retinal dystrophies (RD) characterized by photoreceptor degeneration. RP is highly heterogeneous both clinically and genetically, which complicates the identification of causative genes and mutations. Targeted next-generation sequencing (NGS) has been demonstrated to be an effective strategy for the detection of mutations in RP. In o...
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عنوان ژورنال:
دوره 6 شماره
صفحات -
تاریخ انتشار 2016