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Erratum to: ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies
Author(s) -
Morava Eva,
Tiemes Vera,
Thiel Christian,
Seta Nathalie,
Lonlay Pascale,
Klerk Hans,
Mulder Margot,
RubioGozalbo Estela,
Visser Gepke,
Hasselt Peter,
Horovitz Dafne D. G.,
Souza Carolina Fischinger Moura,
Schwartz Ida V. D.,
Green Andrew,
AlOwain Mohammed,
Uziel Graciella,
Sigaudy Sabine,
Chabrol Brigitte,
Spronsen FrancJan,
Steinert Martin,
Komini Eleni,
Wurm Donald,
Bevot Andrea,
Ayadi Addelkarim,
Huijben Karin,
Dercksen Marli,
Witters Peter,
Jaeken Jaak,
Matthijs Gert,
Lefeber Dirk J.,
Wevers Ron A.
Publication year - 2016
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/s10545-016-9967-4
Subject(s) - ataxia , epilepsy , phenotype , muscle weakness , human genetics , anatomy , medicine , physical medicine and rehabilitation , psychology , neuroscience , genetics , biology , gene