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Merck
CN
  • A novel FTL mutation responsible for neuroferritinopathy with asymmetric clinical features and brain anomalies.

A novel FTL mutation responsible for neuroferritinopathy with asymmetric clinical features and brain anomalies.

Parkinsonism & related disorders (2014-06-08)
Sébastien Moutton, Patricia Fergelot, Jean-Marc Trocello, Violaine Plante-Bordeneuve, Nada Houcinat, Emilie Wenisch, Vincent Larue, Pierre Brugières, Fabienne Clot, Didier Lacombe, Benoit Arveiler, Cyril Goizet
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Sigma-Aldrich
铁蛋白 来源于人类肝脏, Type IV, 10 μg/mL