H63D Syndrome is clinically the iron sibling of Wilson's Disease

H63D Syndrome (all 3 types), is considered a very rare disorder that is difficult to recognize due to its multifaceted nature. Even with homozygous mutation of the HFE gene H63D and the simultaneous presence of the typical clinical symptoms, few clinicians dare to care for affected patients. This is...

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Bibliographische Detailangaben

1. Verfasser:	Stone, Eric
Format:	Dataset
Sprache:	eng
Schlagworte:	H63D Syndrome Medicine, Health and Life Sciences
Online-Zugang:	Volltext bestellen
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