Junko Sakumoto

Familial hypocalciuric hypercalcemia with a de novo heterozygous mutation of calcium-sensing receptor

T. Kogai, A. Hishinuma, K. Taki, 2015, Endocrinology, diabetes & metabolism case reports.

Genetic alteration of ARMC5 in a patient diagnosed with meningioma and primary macronodular adrenal hyperplasia: a case report.

Y. Aso, T. Jojima, T. Kogai, 2020, European journal of endocrinology.

A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation

Y. Aso, T. Jojima, T. Kogai, 2020, Clinical case reports.