Associated Papers
Whole-exome sequencing identifies rare recessive variants in azoospermia patients from consanguineous Pakistani families.
Uddin I et al.
Molecular Genetics and Genomics : Mgg, 2024
The mutation c.346-1G > A in SOHLH1 impairs sperm production in the homozygous but not in the heterozygous condition.
Liu M et al.
Human Molecular Genetics, 2022
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency.
Zhao S et al.
Fertility and Sterility, 2015
Association of genetic variants in SOHLH1 and SOHLH2 with non-obstructive azoospermia risk in the Chinese population.
Song B et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2015
Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death.
Tan ZP et al.
Scientific Reports, 2014
25010007 (PubMed )
Supplement: srep05616-s2.xls › dominant_result_new
Mutations in SOHLH1 gene associate with nonobstructive azoospermia.
Choi Y et al.
Human Mutation, 2010
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