Reply: Hereditary spastic paraplegia caused by a mutation in the VCP gene VCP: A Jack of all trades in neuro-and myodegeneration?

Brain

Volumn 135, Issue 12, 2012, Pages

  Clemen, Christoph S ^a   Eichinger, Ludwig ^a   Schröder, Rolf ^b  

^a UNIVERSITY OF COLOGNE   (Germany)

^b UNIVERSITY HOSPITAL ERLANGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ARGININE; CYSTEINE; STRUMPELLIN; UNCLASSIFIED DRUG; VALOSIN CONTAINING PROTEIN; WISKOTT ALDRICH SYNDROME PROTEIN;

AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; CODON; COGNITIVE DEFECT; DISEASE ASSOCIATION; DNA DAMAGE; ELECTROMYOGRAM; FRONTOTEMPORAL DEMENTIA; GENE DELETION; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; INCLUSION BODY MYOPATHY WITH EARLY ONSET PAGET DISEASE OF BONE AND FRONTOTEMPORAL DEMENTIA; LETTER; MISSENSE MUTATION; MOLECULAR PATHOLOGY; MOLECULAR WEIGHT; MUSCLE ATROPHY; NERVE DEGENERATION; NEUROBIOLOGY; NEUROLOGIC EXAMINATION; PAGET BONE DISEASE; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN DEGRADATION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; RISK FACTOR; WILD TYPE;

EID: 84871792443     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/aws202     Document Type: Letter

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