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Volumn 59, Issue 11, 2002, Pages 1823-
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Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation [4] (multiple letters)
a a a a
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
ALANINE;
MESSENGER RNA;
PROTEIN ALADIN;
PROTEIN DERIVATIVE;
TRIPEPTIDE;
UNCLASSIFIED DRUG;
VALINE;
AAAS GENE;
ACHILLES REFLEX;
ADRENAL INSUFFICIENCY;
ALLGROVE SYNDROME;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
AUTONOMIC DYSFUNCTION;
BABINSKI REFLEX;
BASE PAIRING;
CARBOXY TERMINAL SEQUENCE;
CLINICAL EXAMINATION;
CLINICAL FEATURE;
CODON;
CONSANGUINITY;
DNA SEQUENCE;
DYSARTHRIA;
ELECTROMYOGRAM;
ESOPHAGUS ACHALASIA;
EXON;
FAMILY HISTORY;
GENE;
GENE DELETION;
GENE EXPRESSION;
GENE FUNCTION;
GENE MUTATION;
HOMOZYGOTE;
HUMAN;
HYPERPIGMENTATION;
HYPOGLOSSAL NERVE;
HYPOGLYCEMIA;
KENNEDY DISEASE;
LETTER;
MENTAL DEFICIENCY;
MISSENSE MUTATION;
MOTOR NEUROPATHY;
MUSCLE ATROPHY;
MUSCLE TONE;
MUSCLE WEAKNESS;
MUTATIONAL ANALYSIS;
NERVE CONDUCTION;
NEUROLOGIC EXAMINATION;
NONSENSE MUTATION;
PARALYSIS;
PEDIGREE;
PEROXISOME;
POLYNEUROPATHY;
PRIORITY JOURNAL;
PROTEIN FUNCTION;
PROTEIN PROTEIN INTERACTION;
RNA SPLICING;
RNA STABILITY;
STOP CODON;
SYMPTOM;
TISSUE DISTRIBUTION;
TRANSCRANIAL MAGNETIC STIMULATION;
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EID: 0037058783
PISSN: 00283878
EISSN: None
Source Type: Journal
DOI: 10.1212/WNL.59.11.1823 Document Type: Letter |
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Times cited : (1)
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References (0)
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