Associated Papers
Homozygosity for a novel INHA mutation in two male siblings with hypospadias, primary hypogonadism, and high-normal testicular volume.
Arslan Ates E et al.
European Journal of Endocrinology, 2022
An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures.
Yalçin O et al.
Epilepsia, 2011
Expansion of the germline analysis for the INHA gene in Indian women with ovarian failure.
Dixit H et al.
Human Reproduction (oxford, England), 2006
Identification of Novel Nucleotide Changes in INHBB Gene by Mutation Screening in Females with Ovarian Dysgenesis: A Case Report.
Chauhan P et al.
Journal of Reproduction & Infertility, 0
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