A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotonia
about
Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.Congenital Hyperinsulinism: Diagnosis and Treatment Update.Genetic mechanisms of human hypertension and their implications for blood pressure physiology.Nutrient sensing in pancreatic islets: lessons from congenital hyperinsulinism and monogenic diabetes.Atypical Forms of Congenital Hyperinsulinism in Infancy Are Associated With Mosaic Patterns of Immature Islet Cells.
P2860
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotonia
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
A CACNA1D mutation in a patien ...... defects, and severe hypotonia
@en
A CACNA1D mutation in a patien ...... defects, and severe hypotonia
@nl
type
label
A CACNA1D mutation in a patien ...... defects, and severe hypotonia
@en
A CACNA1D mutation in a patien ...... defects, and severe hypotonia
@nl
prefLabel
A CACNA1D mutation in a patien ...... defects, and severe hypotonia
@en
A CACNA1D mutation in a patien ...... defects, and severe hypotonia
@nl
P2860
P50
P356
P1433
P1476
A CACNA1D mutation in a patien ...... defects, and severe hypotonia
@en
P2093
P2860
P304
P356
10.1111/PEDI.12512
P577
2017-03-20T00:00:00Z