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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

✍ Scribed by Yoshitaka Hayashi; Takashi Kamijo; Michiyo Yamamoto; Yoshiharu Murata; John A. Phillips III; Masamichi Ogawa; Hisao Seo


Book ID
116512175
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
634 KB
Volume
17
Category
Article
ISSN
1096-6374

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