Associated Papers
A novel frameshift variant of GATA3 (p.Ala17ProfsTer178) responsible for HDR syndrome in a Japanese family.
Hasegawa Y et al.
Endocrine Journal, 2024
A GATA3 gene mutation that causes incorrect splicing and HDR syndrome: a case study and literature review.
Tao Y et al.
Frontiers in Genetics, 2023
37693317 (PubMed )
Supplement: Table1.xlsx › Sheet1
Hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome and GATA3.
Horta M et al.
Qjm : Monthly Journal of the Association of Physicians, 2017
Select a paper to view details