Lysosomal abnormalities in hereditary spastic paraplegia types SPG 15 and SPG 11

Author:

Renvoisé Benoît1,Chang Jaerak1,Singh Rajat1,Yonekawa Sayuri2,FitzGibbon Edmond J.3,Mankodi Ami1,Vanderver Adeline4,Schindler Alice B.1,Toro Camilo56,Gahl William A.56,Mahuran Don J.2,Blackstone Craig1,Pierson Tyler Mark167

Affiliation:

1. Neurogenetics Branch National Institute of Neurological Disorders and Stroke National Institutes of Health Bethesda Maryland

2. Research Institute Hospital for Sick Children and University of Toronto Toronto Ontario Canada

3. Laboratory of Sensorimotor Research National Eye Institute National Institutes of Health Bethesda Maryland

4. Department of Neurology Children's National Medical Center Washington District of Columbia

5. Office of the Clinical Director National Human Genome Research Institute National Institutes of Health Bethesda Maryland

6. NIH Undiagnosed Diseases Program National Institutes of Health Office of Rare Diseases Research and National Human Genome Research Institute Bethesda Maryland

7. Departments of Pediatrics and Neurology, and the Regenerative Medicine Institute Cedars‐Sinai Medical Center Los Angeles California

Funder

National Institute of Neurological Disorders and Stroke

National Human Genome Research Institute

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

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