A case with isolated growth hormone deficiency caused by compound heterozygous mutations in GH-1: A novel missense mutation in the initiation codon and a 7.6 kb deletion
| Autor: | Hayashi, Yoshitaka, Kamijo, Takashi, Yamamoto, Michiyo, Murata, Yoshiharu, Phillips, John A., III, Ogawa, Masamichi, Seo, Hisao |
|---|---|
| Zdroj: | In Growth Hormone & IGF Research 2007 17(3):249-253 |
| Databáze: | ScienceDirect |
| Externí odkaz: |
|
Full Text from ScienceDirect