2024-03-29T06:03:00Zhttp://digital.csic.es/dspace-oai/requestoai:digital.csic.es:10261/2112252022-09-14T07:55:32Zcom_10261_22com_10261_1col_10261_401
2020-05-13T07:33:45Z
urn:hdl:10261/211225
Recessive mutations in muscle-specific isoforms of Fxr1 cause congenital multi-minicore myopathy
Estañ, María Cristina
Fernández-Núñez, Elisa
Zaki, Maha S.
Esteban Rodriguez, Isabel
Donkervoort, Sandra
Hawkins, Cynthia
Caparrós-Martín, José A.
Saade, Dimah
Hu, Ying
Bolduc, Véronique
Ru-Yui Chao, Katherine
Nevado, Julian
Lamuedra, Ana
Largo, Raquel
Herrero-Beaumont, Gabriel
Regadera, Javier
Hernández-Chico, Concepción
Tizzano, Eduardo F.
Martinez-Glez, Víctor
Carvajal, Jaime J.
Zong, Ruiting
Nelson, David L.
Otaify, Ghada A.
Temtamy, Samia
Aglan, Mona
Issa, Mahmoud
Bönnemann, Carsten G.
Lapunzina, Pablo
Yoon, Grace
Ruiz-Pérez, Victor L.
Trabajo presentado en la European Society of Human Genetics Conference, celebrada en Göteborg (Suecia) del 15 al 18 de junio de 2019.
2020-05-13T07:33:45Z
2020-05-13T07:33:45Z
2019-06-15
2020-05-13T07:33:45Z
comunicación de congreso
European Society of Human Genetics Conference (2019)
http://hdl.handle.net/10261/211225
Sí
closedAccess