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Kidney International, ISSN 0085-2538, 11/2015, Volume 88, Issue 5, pp. 1153 - 1160
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 06/2019, Volume 34, Issue Supplement_1
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 06/2019, Volume 34, Issue Supplement_1
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 2009, Volume 24, Issue 4, pp. 687 - 696
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 09/2015, Volume 23, Issue 9, pp. 1192 - 1199
Journal Article
Blood, ISSN 0006-4971, 11/2019, Volume 134, Issue Supplement_1, pp. 1099 - 1099
Background: The 50% hemolytic complement (CH50) assay is a non-specific qualitative assay of complement function. CH50 is sometimes used in patients with... 
Journal Article
BMC Nephrology, ISSN 1471-2369, 06/2018, Volume 19, Issue 1, pp. 144 - 5
Journal Article
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 02/2019, Volume 14, Issue 1, pp. 58 - 25
Background: X-linked hypophosphatemia (XLH) is an inherited disease of phosphate metabolism in which inactivating mutations of the Phosphate Regulating... 
MEDICINE, RESEARCH & EXPERIMENTAL | osteomalacia | VITAMIN-D | fibroblast growth factor 23 (FGF23) | hearing impairment | COTRANSPORTER GENE | FIBROBLAST-GROWTH-FACTOR | X-linked hypophosphatemia (XLH) | MOUSE MODEL | GENETICS & HEREDITY | ALKALINE-PHOSPHATASE GENE | dental abscess | bone dysplasia | X-linked (PHEX) | muscle weakness | PHEX MUTATION | vitamin D deficiency | HYP-MOUSE | MURINE MODEL | HEARING-LOSS | phosphate regulating endopeptidase homolog | ectopic calcification | hypophosphatemia | rickets | TRANSGENIC MICE | Complications and side effects | Medical research | Care and treatment | Medicine, Experimental | Hypophosphatemia | Fibroblast growth factors | Research | Fibroblast growth factor | Alkaline phosphatase | Animal models | Disease | Peptides | Fibroblast growth factor 23 | Calcitriol | Arthritis | Proteins | Bone growth | Pain | Rickets | Vitamin D | Fibroblasts | Osteomalacia | Growth factors | 25-Hydroxyvitamin D | Enzymes | Phenotypes | Vitamin deficiency | Hearing impairment | Metabolism | Morbidity | Hereditary diseases | Molecular modelling | Endopeptidase | Abscesses | Calcification | Mutation | Osteoarthritis | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medical Genetics | Medicinsk genetik | Medicinska och farmaceutiska grundvetenskaper | phosphate regulating endopeptidase homolog, X-linked (PHEX)
Journal Article
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