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Autor:
Jesús Argente, Ivon Cuscó, Bhupendra Verma, Mikko J. Frilander, Ali Oghabian, Julie A. Chowen, Gabriel Á. Martos-Moreno, Luis A. Pérez-Jurado, Armand Gutiérrez-Arumí, Raquel Flores
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Recercat. Dipósit de la Recerca de Catalunya
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 6, Iss 3, Pp 299-306 (2014)
instname
Recercat. Dipósit de la Recerca de Catalunya
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 6, Iss 3, Pp 299-306 (2014)
The molecular basis of a significant number of cases of isolated growth hormone deficiency remains unknown. We describe three sisters affected with severe isolated growth hormone deficiency and pituitary hypoplasia caused by biallelic mutations in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::115d38d250e195fa83f4bc8cb0b9de48
http://hdl.handle.net/10486/662774
http://hdl.handle.net/10486/662774