Molecular basis of human growth hormone gene deletions.

Crossover sites resulting from unequal recombination within the human growth hormone (GH) gene cluster that cause GH1 gene deletions and isolated GH deficiency type 1A were localized in nine patients. In eight unrelated subjects homozygous for 6.7-kilobase (kb) deletions, the breakpoints are within...

Description complète

Détails bibliographiques

Publié dans:	Proc Natl Acad Sci U S A
Auteurs principaux:	Vnencak-Jones, C L, Phillips, J A, Chen, E Y, Seeburg, P H
Format:	Artigo
Langue:	Inglês
Publié:	National Academy of Sciences 1988
Sujets:	Research Article
Accès en ligne:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC281810/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2840669/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.85.15.5615
Tags:	Ajouter un tag Pas de tags, Soyez le premier à ajouter un tag!