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Volumn 139, Issue 5, 2016, Pages e28-
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NEK1 mutations in familial amyotrophic lateral sclerosis
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Author keywords
[No Author keywords available]
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Indexed keywords
NEK1 PROTEIN;
PROTEIN SERINE THREONINE KINASE;
UNCLASSIFIED DRUG;
NEK1 PROTEIN, HUMAN;
NIMA RELATED KINASE 1;
SERINE;
THREONINE;
ADULT;
AGED;
AMYOTROPHIC LATERAL SCLEROSIS;
BRAIN ATROPHY;
CONTROLLED STUDY;
DISEASE SEVERITY;
DNA EXTRACTION;
DYSARTHRIA;
DYSPHAGIA;
EXOME;
FAMILIAL DISEASE;
FAMILY;
FEMALE;
FISHER EXACT TEST;
FRAMESHIFT MUTATION;
GENE FREQUENCY;
GENE SEQUENCE;
GENETIC ASSOCIATION;
GENETIC VARIABILITY;
HISTOPATHOLOGY;
HUMAN;
LETTER;
LOSS OF FUNCTION MUTATION;
MAJOR CLINICAL STUDY;
MALE;
MOTONEURON;
NEUROIMAGING;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PRIORITY JOURNAL;
RESPIRATORY FAILURE;
SEGREGATION ANALYSIS;
BRAIN;
COHORT ANALYSIS;
COMPLICATION;
DIAGNOSTIC IMAGING;
FAMILY HEALTH;
GENETICS;
MIDDLE AGED;
MUTATION;
ADULT;
AGED;
AMYOTROPHIC LATERAL SCLEROSIS;
BRAIN;
COHORT STUDIES;
FAMILY HEALTH;
FEMALE;
GENE FREQUENCY;
HUMANS;
MAGNETIC RESONANCE IMAGING;
MALE;
MIDDLE AGED;
MUTATION;
NIMA-RELATED KINASE 1;
RESPIRATORY INSUFFICIENCY;
SERINE;
THREONINE;
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EID: 84966477966
PISSN: 00068950
EISSN: 14602156
Source Type: Journal
DOI: 10.1093/brain/aww033 Document Type: Letter |
Times cited : (109)
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References (9)
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