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Volumn 44, Issue 3, 2012, Pages 254-256
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Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis
a a b a c d e f,g f,g h a a b d i a a a a a more..
d
UNION HOSPITAL
(China)
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Author keywords
[No Author keywords available]
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Indexed keywords
SODIUM PHOSPHATE COTRANSPORTER 3;
ANIMAL CELL;
ARTICLE;
BASAL GANGLION;
BIOASSAY;
FAHR DISEASE;
GENE;
GENE MUTATION;
GENETIC CODE;
MUTANT;
NONHUMAN;
NUCLEOTIDE SEQUENCE;
OOCYTE;
PHOSPHATE METABOLISM;
PHOSPHATE TRANSPORT;
PRIORITY JOURNAL;
SLC20A2 GENE;
XENOPUS LAEVIS;
ANIMALS;
ASIAN CONTINENTAL ANCESTRY GROUP;
BASAL GANGLIA DISEASES;
BASE SEQUENCE;
CALCINOSIS;
CHROMOSOMES, HUMAN, PAIR 8;
GENETIC LINKAGE;
GENETIC MARKERS;
HOMEOSTASIS;
HUMANS;
LOD SCORE;
MOLECULAR SEQUENCE DATA;
MUTATION, MISSENSE;
OOCYTES;
PEDIGREE;
PHOSPHATES;
SEQUENCE ANALYSIS, DNA;
SODIUM-PHOSPHATE COTRANSPORTER PROTEINS, TYPE III;
XENOPUS LAEVIS;
XENOPUS LAEVIS;
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EID: 84862798098
PISSN: 10614036
EISSN: 15461718
Source Type: Journal
DOI: 10.1038/ng.1077 Document Type: Article |
Times cited : (330)
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References (15)
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