✦ LIBER ✦
Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject
✍ Scribed by Lorena Mosca; Christian Lunetta; Claudia Tarlarini; Francesca Avemaria; Eleonora Maestri; Mario Melazzini; Massimo Corbo; Silvana Penco
- Book ID
- 116781904
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 418 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0197-4580
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