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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
Yoshitaka Hayashi, Takashi Kamijo, Michiyo Yamamoto, Yoshiharu Murata, John A. Phillips III, Masamichi Ogawa, Hisao SeoVolume:
17
Year:
2007
Language:
english
DOI:
10.1016/j.ghir.2007.01.019
File:
PDF, 634 KB
english, 2007