Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.

No abstract is available for this paper.

• Publication year

  1999

• Venue

  American Journal of Human Genetics

• Publication date

  1999-02-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1086/302258PMID 9973294PMCID PMC1377766
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1994cited by this paper
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• FAMILY SPASTIC PARALYSIS

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• Beyond motor impairment: investigating cognitive aspects of hereditary spastic paraplegia in a Greek case series.

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• Hereditary spastic paraplegia type 8: Neuropathological findings

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• Combined Treatment Fkt-Botulinum Toxin Type A (Btx-A) in Patients with Strumpell-Lorrain Disease.

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• Chapter 77 – Hereditary Spastic Paraplegia

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• The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8

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• Spastic Paraplegia 8

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• Identification of a new form of autosomal dominant spastic paraplegia

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• Molecular Genetics of Hereditary Spastic Paraplegias

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• A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.

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

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• A clinical, genetic and biochemical study of hereditary spastic paraplegia

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• Chapter 16 Overview on Hereditary Spastic Paraplegias

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  2007cites this paper
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  2006cites this paper
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  2006cites this paper
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  2005cites this paper
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  2002cites this paper
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  2002cites this paper
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  2001cites this paper
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  2000cites this paper
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  2000cites this paper
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  2000cites this paper
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