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1 Ergebnisse
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Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley ..:
Masnada, Silvia
;
Sarret, Catherine
;
Antonello, Clara Eleonora
...
Molecular Genetics and Metabolism. 135 (2022) 1 - p. 109-113 , 2022
Link:
https://doi.org/10.1016/j.ymgme.2021.12.003
RT Journal T1
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ymgme.2021.12.003&Exemplar=1&LAN=DE A1 Masnada, Silvia A1 Sarret, Catherine A1 Antonello, Clara Eleonora A1 Fadilah, Ala A1 Krude, Heiko A1 Mura, Eleonora A1 Mordekar, Santosh A1 Nicita, Francesco A1 Olivotto, Sara A1 Orcesi, Simona A1 Porta, Francesco A1 Remerand, Ganaelle A1 Siri, Barbara A1 Wilpert, Nina-Maria A1 Amir-Yazdani, Pouneh A1 Bertini, Enrico A1 Schuelke, Markus A1 Bernard, Geneviève A1 Boespflug-Tanguy, Odile A1 Tonduti, Davide PB Elsevier BV YR 2022 SN 1096-7192 JF Molecular Genetics and Metabolism VO 135 IS 1 SP 109 OP 113 LK http://dx.doi.org/https://doi.org/10.1016/j.ymgme.2021.12.003 DO https://doi.org/10.1016/j.ymgme.2021.12.003 SF ELIB - SuUB Bremen
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