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pro vyhledávání: '"Ratiba Hannachi"'
Autor:
Marc-Henri de Laet, Annick Rotschild, Rémi Salomon, Clothilde Penet, Stanislas Lyonnet, Ratiba Hannachi, Raja Brauner, Fawzi Bakiri, B. Chaouachi, Jean-Louis Chaussain, Arnold Munnich, Anna Pelet, Smail Hadj-Rabia
Publikováno v:
European Journal of Human Genetics. 8:613-620
Triple A syndrome (Allgrove syndrome, MIM No. 231550) is a rare autosomal recessive disorder characterised by ACTH-resistant adrenal insufficiency, achalasia of the cardia, and alacrimia. The triple A gene has been previously mapped to chromosome 12q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd6bb25063d645e18a8588a450f2c68
https://doi.org/10.1038/sj.ejhg.5200508
https://doi.org/10.1038/sj.ejhg.5200508
