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A novel frameshift PKD1 mutation in a Chinese patient with autosomal dominant polycystic kidney disease and azoospermia: A case report.

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Title: A novel frameshift PKD1 mutation in a Chinese patient with autosomal dominant polycystic kidney disease and azoospermia: A case report.
Authors: Meng, Jialin (AUTHOR), Xu, Yuchen (AUTHOR), Shen, Xufeng (AUTHOR), Liang, Chaozhao (AUTHOR) liang_chaozhao@ahmu.edu.cn
Source: Experimental & Therapeutic Medicine. Jan2019, Vol. 17 Issue 1, p507-511. 5p.
Database: Academic Search Ultimate
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An: 133826811
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  Data: A novel frameshift PKD1 mutation in a Chinese patient with autosomal dominant polycystic kidney disease and azoospermia: A case report.
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  Data: <searchLink fieldCode="AR" term="%22Meng%2C+Jialin%22">Meng, Jialin</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Xu%2C+Yuchen%22">Xu, Yuchen</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Shen%2C+Xufeng%22">Shen, Xufeng</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liang%2C+Chaozhao%22">Liang, Chaozhao</searchLink> (AUTHOR)<i> liang_chaozhao@ahmu.edu.cn</i>
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  Data: <searchLink fieldCode="JN" term="%22Experimental+%26+Therapeutic+Medicine%22">Experimental & Therapeutic Medicine</searchLink>. Jan2019, Vol. 17 Issue 1, p507-511. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=133826811
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      – Code: eng
        Text: English
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        PageCount: 5
        StartPage: 507
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      – TitleFull: A novel frameshift PKD1 mutation in a Chinese patient with autosomal dominant polycystic kidney disease and azoospermia: A case report.
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            NameFull: Meng, Jialin
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            NameFull: Xu, Yuchen
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            NameFull: Shen, Xufeng
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            NameFull: Liang, Chaozhao
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              Text: Jan2019
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              Y: 2019
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              Value: 17
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            – TitleFull: Experimental & Therapeutic Medicine
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