Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Liu-Fei Miao"'
Autor:
Xiao-Jun Li, Bai‐zeng Yu, Wei-Qing Wu, Ying-Xia Cui, Liu-Fei Miao, Fangfang Chen, Jia-Xun Zhang, Xing Lv, Zheng-Kun Xia, Zhi-Hong Liu
Publikováno v:
Cytogenetic and Genome Research. 160:238-244
X-linked Alport syndrome (XLAS) is a common hereditary nephropathy caused by COL4A5 gene mutations. To date, many splice site mutations have been described but few have been functionally analyzed to verify the exact splicing effects that contribute t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::819faf6554406f630c6b258772989c67
https://doi.org/10.1159/000508562
https://doi.org/10.1159/000508562
Autor:
Xing, Lv, Wei-Qing, Wu, Jia-Xun, Zhang, Liu-Fei, Miao, Bai-Zeng, Yu, Fang-Fang, Chen, Ying-Xia, Cui, Zheng-Kun, Xia, Zhi-Hong, Liu, Xiao-Jun, Li
Publikováno v:
Cytogenetic and genome research. 160(5)
X-linked Alport syndrome (XLAS) is a common hereditary nephropathy caused by COL4A5 gene mutations. To date, many splice site mutations have been described but few have been functionally analyzed to verify the exact splicing effects that contribute t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ec9ccc9679989f6e3932440e8fe93cc
https://pubmed.ncbi.nlm.nih.gov/32659759
https://pubmed.ncbi.nlm.nih.gov/32659759