Shima, Hirohito

SOX2 nonsense mutation in a patient clinically diagnosed with non-syndromic hypogonadotropic hypogonadism. [electronic resource] - Endocrine journal Aug 2017 - 813-817 p. digital

Publication Type: Case Reports; Journal Article

1348-4540

10.1507/endocrj.EJ17-0078 doi


Codon, Nonsense
DNA Mutational Analysis
Humans
Hypogonadism--genetics
Male
Phenotype
SOXB1 Transcription Factors--genetics
Young Adult