Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description-Reference-Cited by-同舟云学术

Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description

Published:2007-05-14 Issue:7 Volume:144B Page:854-861
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Klebe Stephan¹²,Durr Alexandra¹²³⁴,Bouslam Naima¹⁵,Grid Djamel⁶,Paternotte Caroline⁷,Depienne Christel¹²³⁴,Hanein Sylvain¹²,Bouhouche Ahmed⁵,Elleuch Nizar¹²,Azzedine Hamid¹²³,Poea‐Guyon Sandrine¹,Forlani Sylvie¹²³,Denis Elodie¹²³,Charon Céline⁸,Hazan Jamile⁷⁹,Brice Alexis¹²³⁴¹⁰,Stevanin Giovanni¹²³⁴

Affiliation:

1. INSERM, U679, Paris, France

2. Pierre and Marie Curie‐Paris6 University, UMR S679, Pitié‐Salpêtrière Hospital, Paris, France

3. Federative Institute for Neuroscience Research (IFR70), Pitié‐Salpêtrière Hospital, Paris, France

4. AP‐HP, Pitié‐Salpêtrière Hospital, Department of Genetics and Cytogenetics, Paris, France

5. Neurology B and Neurogenetics unit, Specialties hospital, Rabat, Morocco

6. Généthon, Evry, France

7. Genoscope, CNS, Evry, France

8. National Genotyping Center, Evry, France

9. Centre for Developmental Neurobiology, King's College London, Guy's Hospital Campus, United Kingdom

10. AP‐HP, Pitié‐Salpêtrière Hospital, Federation of Neurology, Paris, France

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.30518

Reference37 articles.

1. A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32

2. Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)

3. Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

4. Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias

5. The Troyer Syndrome

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