NovelB4GALNT1mutations in a complicated form of hereditary spastic paraplegia-Reference-Cited by-同舟云学术

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NovelB4GALNT1mutations in a complicated form of hereditary spastic paraplegia

Published:2013-11-27 Issue:5 Volume:86 Page:500-501
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Wakil S.M.¹,Monies D.M.¹,Ramzan K.¹,Hagos S.¹,Bastaki L.²,Meyer B.F.¹,Bohlega S.³

Affiliation:

1. Department of Genetics; King Faisal Specialist Hospital and Research Centre; Riyadh Saudi Arabia

2. Department of Clinical Genetics; Kuwait Medical Genetics Centre; Kuwait

3. Department of Neurosciences; King Faisal Specialist Hospital and Research Centre; Riyadh Saudi Arabia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference5 articles.

1. Recent advances in the genetics of spastic paraplegias;Stevanin;Curr Neurol Neurosci Rep,2008

2. A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14;Wilkinson;J Med Genet,2005

3. Biosynthesis and functions of gangliosides: recent advances;Lloyd;Glycoconj J,1998

4. Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase;Simpson;Nat Genet,2004

5. Alteration of ganglioside biosynthesis for complex hereditary spastic paraplegia;Boukhris;Am J Hum Genet,2013

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