A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3-Reference-Cited by-同舟云学术

A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3

Published:2007-06-28 Issue:3-4 Volume:122 Page:261-273
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Hanein Sylvain,Dürr Alexandra,Ribai Pascale,Forlani Sylvie,Leutenegger Anne-Louise,Nelson Isabelle,Babron Marie-Claude,Elleuch Nizar,Depienne Christel,Charon Céline,Brice Alexis,Stevanin Giovanni

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-007-0396-1.pdf

Reference48 articles.

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4. Cottingham RW Jr, Idury RM, Schaffer AA (1993) Faster sequential genetic linkage computations. Am J Hum Genet 53:252–263

5. D’Amico A, Tessa A, Sabino A, Bertini E, Santorelli FM, Servidei S (2004) Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene. Neurology 62:2138–2139

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