Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect-Reference-Cited by-同舟云学术

Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect

Published:2005-12-22 Issue:2 Volume:59 Page:398-403
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Lee Jennifer A.¹,Madrid Ricardo E.²,Sperle Karen³,Ritterson Carolyn M.⁴,Hobson Grace M.³⁵,Garbern James⁶,Lupski James R.¹⁷⁸,Inoue Ken¹⁹

Affiliation:

1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX

2. New York State Institute for Basic Research in Developmental Disabilities, George A. Jervis Clinic, Staten Island, NY

3. Nemours Biomedical Research, Alfred I. duPont Hospital for Children, Nemours Children's Clinic, Wilmington, DE

4. Department of Biology, Boston University, Boston, MA

5. Department of Pediatrics, Jefferson Medical College, Philadelphia, PA

6. Department of Neurology and Center of Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI

7. Department of Pediatrics, Baylor College of Medicine, Houston, TX

8. Texas Children's Hospital, Houston, TX

9. Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan

Funder

Muscular Dystrophy Association

Nervous and Mental Disorders from Ministry of Health, Labor and Welfare

NIH

National Institute for Child Health and Development

New York State Office of Mental Retardation and Developmental Disabilities

Nemours Foundation

PMD Foundation

Kylan Hunter Foundation

NIH National Center for Research Resources

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.20732

Reference21 articles.

1. The Molecular Pathogenesis of Pelizaeus-Merzbacher Disease

3. Proteolipid protein gene duplications causing Pelizaeus-Merzbacher disease: Molecular mechanism and phenotypic manifestations

4. Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

5. Proteolipid Protein Is Necessary in Peripheral as Well as Central Myelin

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