Clinical and genetic analysis of four Taiwanese families with autosomal dominant hereditary spastic paraplegia

Hereditary spastic paraplegias (HSPs) are clinically and genetically heterogeneous neurodegenerative disorders. Defects in the SPG4 and SPG3A genes are the two leading causes of HSPs with autosomal dominant inheritance (AD-HSPs). The purpose of this study was to investigate the clinical features and...

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Bibliografische gegevens
Hoofdauteurs:	Min-Yu Lan, Ser-Chen Fu, Yung-Yee Chang, Yah-Huei Wu-Chou, Szu-Chia Lai, Rou-Shyan Chen, Chin-Song Lu
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	Elsevier 2012-07-01
Reeks:	Journal of the Formosan Medical Association
Onderwerpen:	hereditary spastic paraplegia multiplex ligation-dependent probe amplification SPG4 spastin
Online toegang:	http://www.sciencedirect.com/science/article/pii/S0929664612000599
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Clinical and genetic analysis of four Taiwanese families with autosomal dominant hereditary spastic paraplegia

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