A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings.
Journal of Clinical Research in Pediatric Endocrinology, 2023 - europepmc.org
Transaldolase deficiency is a rare inborn autosomal recessive disorder caused by biallelic
mutations in the TALDO1 gene. It is characterized by intrauterine growth restriction …
mutations in the TALDO1 gene. It is characterized by intrauterine growth restriction …
A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings
M Yildiz, Z Onal, G Yesil, T Goksu Kabil, G Toksoy - JOURNAL OF CLINICAL … - jcrpe.org
Transaldolase deficiency is a rare inborn autosomal recessive disorder caused by biallelic
mutations in the TALDO1 gene. It is characterized by intrauterine growth restriction …
mutations in the TALDO1 gene. It is characterized by intrauterine growth restriction …
A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings
M Yildiz, Z Onal, G Yesil, TG Kabil… - Journal of clinical … - pubmed.ncbi.nlm.nih.gov
Transaldolase deficiency is a rare inborn autosomal recessive disorder caused by biallelic
mutations in the TALDO1 gene. It is characterized by intrauterine growth restriction …
mutations in the TALDO1 gene. It is characterized by intrauterine growth restriction …