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SYCE1
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Body Atlas
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Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian ins…
Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insuffic…
Novel Mutations Reduce Expression of Meiotic Regulators SYCE1 and BOLL in Testis of Azoospermic Men …
Novel exon mutation in SYCE1 gene is associated with non-obstructive azoospermia.
Syce1 and Syce3 regulate testosterone and dihydrotestosterone synthesis via steroidogenic pathways i…
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