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A Correlation between EGFR Gene Mutation Status and Bronchioloalveolar Carcinoma Features in Japanese Patients with Adenocarcinoma

✍ Scribed by Haneda, H.


Book ID
118042603
Publisher
Oxford University Press
Year
2006
Tongue
English
Weight
102 KB
Volume
36
Category
Article
ISSN
0368-2811

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## Abstract Neuroferritinopathy is a hereditary neurodegenerative disorder caused by mutations in the ferritin light chain gene (__FTL1__). The cardinal features are progressive movement disturbance, hypoferritinemia, and iron deposition in the brain. To date, five mutations have been described in