## Abstract Huntington's disease (HD) classically presents with movement disorder, cognitive dysfunction and behavioral problems but is phenotypically variable. One percent of patients with HDβlike symptoms lack the causative mutation and are considered HD phenocopies. Genetic diseases known to cau
β¦ LIBER β¦
Genetic and clinical heterogeneity of ferroportin disease
β Scribed by Laura Cemonesi; Gian Luca Forni; Nadia Soriani; Martina Lamagna; Isabella Fermo; Filomena Daraio; Anna Galli; Daniela Pietra; Luca Malcovati; Maurizio Ferrari; Clara Camaschella; Mario Cazzola
- Book ID
- 108673498
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 345 KB
- Volume
- 131
- Category
- Article
- ISSN
- 0007-1048
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