Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Carla Munné-Miralvés"'
Autor:
Carla Munné-Miralvés, Lluís Brunet-Llobet, Abel Cahuana-Cárdenas, Sergi Torné-Durán, Jaume Miranda-Rius, Alejandro Rivera-Baró
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Abstract Introduction Prader-Willi Syndrome (PWS) is a genetic disorder caused by the lack of expression of certain paternal genes located on chromosome 15q11-q13. This anomaly causes cognitive, neurological and endocrine abnormalities, among which o
Externí odkaz:
https://doaj.org/article/e4a4ac76efc8498a8ee90c78da8a8ab4
Autor:
Lluís Brunet-Llobet, Abel Cahuana-Cárdenas, Alejandro Rivera-Baró, Jaume Miranda-Rius, Carla Munné-Miralvés, Sergi Torné-Duran
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Orphanet Journal of Rare Diseases
Dipòsit Digital de la UB
Universidad de Barcelona
Orphanet Journal of Rare Diseases
Dipòsit Digital de la UB
Universidad de Barcelona
Introduction Prader-Willi Syndrome (PWS) is a genetic disorder caused by the lack of expression of certain paternal genes located on chromosome 15q11-q13. This anomaly causes cognitive, neurological and endocrine abnormalities, among which one of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dee9662235efad67c79166a9e8562e39
https://doaj.org/article/e4a4ac76efc8498a8ee90c78da8a8ab4
https://doaj.org/article/e4a4ac76efc8498a8ee90c78da8a8ab4