✦ LIBER ✦

A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia

✍ Scribed by Roneil Malkani; Ian D'Souza; Katrina Gwinn-Hardy; Gerard D. Schellenberg; John Hardy; Parastoo Momeni

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutation in the tau exon 10 splice site

✍ H. R. Morris; J. Perez-Tur; J. C. Janssen; J. Brown; A. J. Lees; N. W. Wood; J. 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 216 KB 👁 2 views

We are grateful to Drs C. Clough and T. Fowler for allowing us to study their patients.

CHMP2B mutations are not a cause of deme

✍ Patrizia Rizzu; Saskia E. van Mil; Burcu Anar; Sonia M. Rosso; Laura Donker Kaat 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 51 KB 👁 2 views

Familial frontotemporal dementia and par

✍ Eizo Iseki; Takehiko Matsumura; Wami Marui; Hiroaki Hino; Toshinari Odawara; Nao 📂 Article 📅 2001 🏛 Springer-Verlag 🌐 English ⚖ 420 KB

Heterogeneous nuclear ribonucleoprotein

✍ Yan Wang; Lei Gao; Sze-Wah Tse; Athena Andreadis 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 985 KB

Compound heterozygosity for a premature

✍ T-W Kang; S-W Oh; M-R Kim; JS Lee; S-C Kim 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 558 KB