SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome.
about
NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.The dual role of MamB in magnetosome membrane assembly and magnetite biomineralization.A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers.Zinc Transporter Proteins.Progranulin Deficient Mice Develop Nephrogenic Diabetes Insipidus
P2860
SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
SLC30A9 mutation affecting int ...... novel cerebro-renal syndrome.
@en
SLC30A9 mutation affecting int ...... novel cerebro-renal syndrome.
@nl
type
label
SLC30A9 mutation affecting int ...... novel cerebro-renal syndrome.
@en
SLC30A9 mutation affecting int ...... novel cerebro-renal syndrome.
@nl
prefLabel
SLC30A9 mutation affecting int ...... novel cerebro-renal syndrome.
@en
SLC30A9 mutation affecting int ...... novel cerebro-renal syndrome.
@nl
P2093
P2860
P50
P356
P1433
P1476
SLC30A9 mutation affecting int ...... novel cerebro-renal syndrome.
@en
P2093
Daniel Landau
Evgenia Gurevich
Hanna Shalev
Keren Liani-Leibson
Libe Gradstein
Michael Volodarsky
Pauline Chabosseau
Rotem Kadir
Ruth Schreiber
Shiran Barber-Zucker
P2860
P304
P356
10.1093/BRAIN/AWX013
P407
P577
2017-04-01T00:00:00Z