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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.

UniProtKB (1) rdf/xml

Igarashi Y., Ogawa M., Kamijo T., Iwatani N., Nishi Y., Kohno H., Masumura T., Koga J.

Hum. Mol. Genet. 2:1073-1074(1993) [PubMed] [Europe PMC]