Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action.
about
A 23-year-old patient with secondary tumoral calcinosis: Regression after subtotal parathyroidectomy: A case reportDialysis as a Treatment Option for a Patient With Normal Kidney Function and Familial Tumoral Calcinosis Due to a Compound Heterozygous FGF23 Mutation.Clinical Utility Gene Card For: GALNT3 defective congenital disorder of glycosylation.
P2860
Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action.
@en
type
label
Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action.
@en
prefLabel
Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action.
@en
P2860
P1476
Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action.
@en
P2093
Erik A Imel
Lisal J Folsom
P2860
P2888
P356
10.1007/S11914-015-0254-3
P577
2015-04-01T00:00:00Z
P6179
1004452284