Exome Sequencing in the Clinical Diagnosis of Sporadic or Familial Cerebellar Ataxia

Author:

Fogel Brent L.1,Lee Hane2,Deignan Joshua L.2,Strom Samuel P.2,Kantarci Sibel2,Wang Xizhe1,Quintero-Rivera Fabiola2,Vilain Eric3,Grody Wayne W.4,Perlman Susan1,Geschwind Daniel H.5,Nelson Stanley F.6

Affiliation:

1. Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles

2. Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles3UCLA Clinical Genomics Center, David Geffen School of Medicine, University of California at Los Angeles

3. UCLA Clinical Genomics Center, David Geffen School of Medicine, University of California at Los Angeles4Department of Human Genetics, David Geffen School of Medicine, University of California at Los Angeles5Department of Pediatrics, David Geffen School of

4. Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles3UCLA Clinical Genomics Center, David Geffen School of Medicine, University of California at Los Angeles4Department of Human Genetics,

5. Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles4Department of Human Genetics, David Geffen School of Medicine, University of California at Los Angeles

6. Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles2Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles3UCLA Clin

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical)

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