A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones

Julia Winter, Olaf Hiort, Pia Hermanns, Susanne Thiele, Joachim Pohlenz*

*Corresponding author for this work
3 Citations (Scopus)

Fingerprint

Dive into the research topics of 'A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones'. Together they form a unique fingerprint.

Biochemistry, Genetics and Molecular Biology