A novel MKRN3 nonsense mutation causing familial central precocious puberty.
| Title | A novel MKRN3 nonsense mutation causing familial central precocious puberty. |
| Publication Type | Journal Article |
| Year of Publication | 2017 |
| Authors | Christoforidis, A., Skordis N., Fanis P., Dimitriadou M., Sevastidou M., Phelan M. M., Neocleous V., & Phylactou L. A. |
| Journal | Endocrine |
| Volume | 56 |
| Issue | 2 |
| Pagination | 446-449 |
| Date Published | 2017 May |
| ISSN | 1559-0100 |
| Keywords | Amino Acid Substitution, Child, Codon, Nonsense, DNA Mutational Analysis, Fathers, Female, Heterozygote, Humans, Pedigree, Puberty, Precocious, Ribonucleoproteins, Sex Distribution, Siblings |
| DOI | 10.1007/s12020-017-1232-6 |
| Alternate Journal | Endocrine |
| PubMed ID | 28132164 |
