A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene
Year: 1993
Type: article
Source: Human Molecular Genetics
DOI: 10.1093/hmg/2.7.1073
Authors: Yutaka Igarashi, Masamichi Ogawa, Takashi Kamijo, Noritaka Iwatani, Yoshikazu Nishi, Hitoshi Kohno, Takehiro Masumura, Junichi Koga
Institutions: Nagoya University, JCR Pharmaceuticals (Japan)
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2111908264