Search Results - Ríos‐Ocampo, W. Alfredo

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    Mutations in the V-ATPase assembly factor VMA21 cause a congenital disorder of glycosylation with autophagic liver disease by Cannata Serio, Magda (Author) , Graham, Laurie A. (Author) , Ashikov, Angel (Author) , Larsen, Lars Elmann (Author) , Raymond, Kimiyo (Author) , Timal, Sharita (Author) , Meur, Gwenn Le (Author) , Ryan, Margret (Author) , Czarnowska, Elzbieta (Author) , Jansen, Jos C. (Author) , He, Miao (Author) , Ficicioglu, Can (Author) , Pichurin, Pavel (Author) , Hasadsri, Linda (Author) , Minassian, Berge (Author) , Rugierri, Alessandra (Author) , Kalimo, Hannu (Author) , Ríos‐Ocampo, W. Alfredo (Author) , Gilissen, Christian (Author) , Rodenburg, Richard (Author) , Jonker, Johan W. (Author) , Holleboom, Adriaan G. (Author) , Morava, Eva (Author) , Veltman, Joris A. (Author) , Socha, Piotr (Author) , Stevens, Tom H. (Author) , Simons, Matias (Author) , Lefeber, Dirk J. (Author) ,


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