✦ LIBER ✦

Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia

✍ Scribed by Kirsten Svenstrup; Peter Bross; Pernille Koefoed; Lena E. Hjermind; Hans Eiberg; A. Peter Born; John Vissing; Jesper Gyllenborg; Anne Nørremølle; Lis Hasholt; Jørgen E. Nielsen

Book ID: 119303396
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 236 KB
Volume: 284
Category: Article
ISSN: 0022-510X
DOI: 10.1016/j.jns.2009.04.024

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

SPAST mutations in Australian patients w

SPAST mutations in Australian patients with hereditary spastic paraplegia

✍ Vandebona, H.; Kerr, N. P.; Liang, C.; Sue, C. M. 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 106 KB

0217 Novel mutation in the gene SPG3A in

0217 Novel mutation in the gene SPG3A in hereditary spastic paraplegia

📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 129 KB

High frequency of partial SPAST deletion

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia

✍ Beetz, C.; Nygren, A.O.H.; Schickel, J.; Auer-Grumbach, M.; Burk, K.; Heide, G.; 📂 Article 📅 2006 🏛 Lippincott Williams and Wilkins 🌐 English ⚖ 515 KB

Novel SPG3A and SPG4 mutations in domina

Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families

✍ J. L. Loureiro; L. Miller-Fleming; C. Thieleke-Matos; P. Magalhães; V. T. Cruz; 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB

Mutational spectrum of theSPG4(SPAST) an

Mutational spectrum of theSPG4(SPAST) andSPG3A(ATL1) genes in Spanish patients with hereditary spastic paraplegia

✍ Victoria Álvarez; Elena Sánchez-Ferrero; Christian Beetz; Marta Díaz; Belén Alon 📂 Article 📅 2010 🏛 BioMed Central 🌐 English ⚖ 677 KB

SPG3A mutation screening in English fami

SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia

✍ P.A. Wilkinson; P.E. Hart; H. Patel; T.T. Warner; A.H. Crosby 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 171 KB