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Clinical and molecular diagnosis of non‐phosphomannomutase ..:
Medrano, Celia
;
Vega, Ana
;
Navarrete, Rosa
...
Clinical Genetics. 95 (2019) 5 - p. 615-626 , 2019
Link:
https://doi.org/10.1111/cge.13508
RT Journal T1
Clinical and molecular diagnosis of non‐phosphomannomutase 2 N‐linked congenital disorders of glycosylation in Spain
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.13508&Exemplar=1&LAN=DE A1 Medrano, Celia A1 Vega, Ana A1 Navarrete, Rosa A1 Ecay, M. Jesús A1 Calvo, Rocío A1 Pascual, Samuel Ignacio A1 Ruiz‐Pons, Mónica A1 Toledo, Laura A1 García‐Jiménez, Inmaculada A1 Arroyo, Ignacio A1 Campo, Andrea A1 Couce, M. Luz A1 Domingo‐Jiménez, M. Rosario A1 García‐Silva, M. Teresa A1 González‐Gutiérrez‐Solana, Luis A1 Hierro, Loreto A1 Martín‐Hernández, Elena A1 Martínez‐Pardo, Mercedes A1 Roldán, Susana A1 Tomás, Miguel A1 Cabrera, Jose C. A1 Mártinez‐Bugallo, Francisco A1 Martín‐Viota, Lucía A1 Vitoria‐Miñana, Isidro A1 Lefeber, Dirk J. A1 Girós, M. Luisa A1 Serrano Gimare, Mercedes A1 Ugarte, Magdalena A1 Pérez, Belén A1 Pérez‐Cerdá, Celia PB Wiley YR 2019 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 95 IS 5 SP 615 OP 626 LK http://dx.doi.org/https://doi.org/10.1111/cge.13508 DO https://doi.org/10.1111/cge.13508 SF ELIB - SuUB Bremen
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