Loss of function of Slc20a2 associated with familial idiopathic basal ganglia calcification in humans causes brain calcifications in mice

Journal of Molecular Neuroscience

Volumn 51, Issue 3, 2013, Pages 994-999

  Jensen, Nina ^a   Schrøder, Henrik Daa ^c   Hejbøl, Eva Kildall ^c   Füchtbauer, Ernst Martin ^a   De Oliveira, João Ricardo Mendes ^d   Pedersen, Lene ^a,b  

^a AARHUS UNIVERSITY   (Denmark)

^b AARHUS UNIVERSITY HOSPITAL   (Denmark)

^c ODENSE UNIVERSITY HOSPITAL   (Denmark)

^d FEDERAL UNIVERSITY OF PERNAMBUCO   (Brazil)

Author keywords

Brain calcification; Phosphate transporter; PiT2; SLC20A2

Indexed keywords

MEMBRANE PROTEIN; PROTEIN SLC20A2; SODIUM PHOSPHATE COTRANSPORTER; TYPE III SODIUM DEPENDENT PHOSPHATE TRANSPORTER 2; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BASAL GANGLION; BRAIN CALCIFICATION; BRAIN CORTEX; CONTROLLED STUDY; FAHR DISEASE; FAMILIAL IDIOPATHIC BASAL GANGLIA CALCIFICATION; FEMALE; GENOTYPE; HISTOLOGY; HOMOZYGOTE; LOSS OF FUNCTION MUTATION; MALE; MOUSE; NONHUMAN; QUANTITATIVE ANALYSIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; THALAMUS;

MUS;

ANIMALS; BASAL GANGLIA DISEASES; BRAIN; CALCINOSIS; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; NEURODEGENERATIVE DISEASES; SODIUM-PHOSPHATE COTRANSPORTER PROTEINS, TYPE III;

EID: 84885948431     PISSN: 08958696     EISSN: 15591166     Source Type: Journal    
DOI: 10.1007/s12031-013-0085-6     Document Type: Article

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