A novel frameshift PKD1 mutation in a Chinese patient with autosomal dominant polycystic kidney disease and azoospermia: A case report.
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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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2018 nî lūn-bûn
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2018年の論文
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2018年学术文章
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2018年学术文章
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2018年学术文章
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2018年学术文章
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2018年學術文章
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2018年學術文章
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name
A novel frameshift PKD1 mutati ...... nd azoospermia: A case report.
@en
A novel frameshift PKD1 mutati ...... nd azoospermia: A case report.
@nl
type
label
A novel frameshift PKD1 mutati ...... nd azoospermia: A case report.
@en
A novel frameshift PKD1 mutati ...... nd azoospermia: A case report.
@nl
prefLabel
A novel frameshift PKD1 mutati ...... nd azoospermia: A case report.
@en
A novel frameshift PKD1 mutati ...... nd azoospermia: A case report.
@nl
P356
P1476
A novel frameshift PKD1 mutati ...... nd azoospermia: A case report.
@en
P2093
Xufeng Shen
P304
P356
10.3892/ETM.2018.6946
P577
2018-11-09T00:00:00Z