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.
作者信息
Igarashi Y, Ogawa M, Kamijo T, Iwatani N, Nishi Y, Kohno H, Masumura T, Koga J
机构信息
Department of Pediatrics, Nagoya University School of Medicine, Japan.
出版信息
Hum Mol Genet. 1993 Jul;2(7):1073-4. doi: 10.1093/hmg/2.7.1073.
PMID:8364549
Abstract
摘要
Zotero 插件