Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lianmei Zhang"'
Autor:
Chunli Wei, Hongbin Lv, Lianmei Zhang, Jiewen Fu, Qi Zhou, Junjiang Fu, Songyot Anuchapreeda, Jingliang Cheng, Shamsuddin Sultan Khan
Publikováno v:
3 Biotech. 11
Retinitis pigmentosa (RP) is a rare and heterogeneous group of inherited ocular diseases. However, the relationship between CACNA2D4 mutations and RP is not well understood. In this study, a Chinese autosomal recessive retinitis pigmentosa (arRP) ped
Autor:
Jingliang, Cheng, Qi, Zhou, Jiewen, Fu, Chunli, Wei, Lianmei, Zhang, Md Shamsuddin Sultan, Khan, Hongbin, Lv, Songyot, Anuchapreeda, Junjiang, Fu
Publikováno v:
3 Biotech
Retinitis pigmentosa (RP) is a rare and heterogeneous group of inherited ocular diseases. However, the relationship between CACNA2D4 mutations and RP is not well understood. In this study, a Chinese autosomal recessive retinitis pigmentosa (arRP) ped
Autor:
Lianmei Zhang, Jingliang Cheng, Qi Zhou, Md. Asaduzzaman Khan, Jiewen Fu, Chengxia Duan, Suan Sun, Hongbin Lv, Junjiang Fu
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics, Vol 11 (2020)
Usher syndrome includes a group of genetically and clinically heterogeneous autosomal recessive diseases, such as retinitis pigmentosa (RP) and sensorineural hearing loss. Usher syndrome type I (USHI) is characterized by profound hearing impairment b