## Abstract Neuroferritinopathy is a recently recognized autosomal dominant disorder that results in abnormal aggregates of iron and ferritin in the brain due to a mutation in the ferritin light chain gene on chromosome 19q13.3. We present the clinical details of a patient with adultβonset generali
Adult-onset leg dystonia due to a missense mutation in THAP1
β Scribed by Jay A. Van Gerpen; Mark S. LeDoux; Zbigniew K. Wszolek
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 599 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
β¦ Synopsis
Nothing to disclose. Author Roles: Mohammed T. Ahmad was involved in the writing of the first draft, patient assessment, followup, and video filming. Kumar M. Prakash was involved in review and critique, writing of the final draft, patient and video assessment, and video editing.
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