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Volumn 23, Issue 5, 2012, Pages 1038-1042
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Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRPM6 gene mutation.
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Author keywords
[No Author keywords available]
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Indexed keywords
BIOLOGICAL MARKER;
MAGNESIUM;
MAGNESIUM SULFATE;
TRANSIENT RECEPTOR POTENTIAL CHANNEL M;
TRPM6 PROTEIN, HUMAN;
ARTICLE;
BLOOD;
CALCINOSIS;
CASE REPORT;
COMPUTER ASSISTED TOMOGRAPHY;
EXTRAPYRAMIDAL SYNDROME;
FEMALE;
FRAMESHIFT MUTATION;
GENETIC PREDISPOSITION;
GENETICS;
HOMOZYGOTE;
HUMAN;
HYPOCALCEMIA;
INFANT;
KIDNEY TUBULE DISORDER;
NUCLEOTIDE SEQUENCE;
PHENOTYPE;
SEIZURE;
TREATMENT OUTCOME;
BASAL GANGLIA DISEASES;
BIOLOGICAL MARKERS;
CALCINOSIS;
DNA MUTATIONAL ANALYSIS;
FEMALE;
FRAMESHIFT MUTATION;
GENETIC PREDISPOSITION TO DISEASE;
HOMOZYGOTE;
HUMANS;
HYPOCALCEMIA;
INFANT;
MAGNESIUM;
MAGNESIUM SULFATE;
PHENOTYPE;
RENAL TUBULAR TRANSPORT, INBORN ERRORS;
SEIZURES;
TOMOGRAPHY, X-RAY COMPUTED;
TREATMENT OUTCOME;
TRPM CATION CHANNELS;
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EID: 84873256099
PISSN: 13192442
EISSN: None
Source Type: Journal
DOI: 10.4103/1319-2442.100945 Document Type: Article |
Times cited : (15)
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References (0)
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