The DAX1 mutation in a patient with hypogonadotropic hypogonadism and adrenal hypoplasia congenita causes functional disruption of induction of spermatogenesis.
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A Novel Mutation of DAX-1 Associated with Secretory Azoospermia.Perspectives in Pediatric Pathology, Chapter 22. Testicular Involvement in Systemic Diseases.Novel mutations of DAX1 (NR0B1) in two Chinese families with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.CRISPR/Cas9-mediated Dax1 knockout in the monkey recapitulates human AHC-HH.
P2860
The DAX1 mutation in a patient with hypogonadotropic hypogonadism and adrenal hypoplasia congenita causes functional disruption of induction of spermatogenesis.
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2012 nî lūn-bûn
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2012年の論文
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The DAX1 mutation in a patient ...... induction of spermatogenesis.
@en
The DAX1 mutation in a patient ...... induction of spermatogenesis.
@nl
type
label
The DAX1 mutation in a patient ...... induction of spermatogenesis.
@en
The DAX1 mutation in a patient ...... induction of spermatogenesis.
@nl
prefLabel
The DAX1 mutation in a patient ...... induction of spermatogenesis.
@en
The DAX1 mutation in a patient ...... induction of spermatogenesis.
@nl
P2093
P2860
P1476
The DAX1 mutation in a patient ...... induction of spermatogenesis.
@en
P2093
Donata Ponikwicka-Tyszko
Katarzyna Jarzabek
Malgorzata Kotula-Balak
Slawomir Wolczynski
P2860
P2888
P304
P356
10.1007/S10815-012-9778-Y
P577
2012-05-05T00:00:00Z
P5875
P6179
1044037667