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