Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosis.
第一作者:
Abbhirami,Rajagopal
第一单位:
Department of Molecular and Human Genetics (A.R., D.L., R.G., P.C., B.L.), Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030; Centro de Investigaciones Endocrinológicas "Dr. César Bergadá" (CEDIE) (D.B., F.C., H.C., I.B.), CONICET - FEI - División de Endocrinología, Hospital de Niños Ricardo Gutiérrez, C1425FD Buenos Aires, Argentina; Human Genome Sequencing Center (J.T.L., R.G.), Department of Structural and Computational Biology and Molecular Biophysics (J.T.L.), Baylor College of Medicine, Houston, Texas 77030; Unidad de Metabolismo (S.K.), Hospital de Niños Ricardo Gutiérrez, C1425FD Buenos Aires, Argentina; Unidad de Nefrología (J.M.L., G.V.), Hospital de Niños Ricardo Gutiérrez, C1425FD Buenos Aires, Argentina; Howard Hughes Medical Institute (B.L.), Houston, Texas 77030.
作者:
医学主题词
儿童(Child);儿童, 学龄前(Child, Preschool);DNA突变分析(DNA Mutational Analysis);女(雌)性(Female);人类(Humans);高钙血症(Hypercalcemia);高钙尿症(Hypercalciuria);低磷血症(Hypophosphatemia);男(雄)性(Male);突变(Mutation);肾钙质沉着症(Nephrocalcinosis);甲状旁腺素(Parathyroid Hormone);系谱(Pedigree);表型(Phenotype);钠-磷协同转运蛋白质类, Ⅱa型(Sodium-Phosphate Cotransporter Proteins, Type IIa)
DOI
10.1210/jc.2014-1517
PMID
25050900
发布时间
2022-04-08
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