Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension.
about
ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment.ADAMTS13 missense variants associated with defective activity and secretion of ADAMTS13 in a patient with non-cirrhotic portal hypertension.Mutations in the novel gene FOPV are associated with familial autosomal dominant and non-familial obliterative portal venopathy.
P2860
Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Recurrent recessive mutation i ...... cirrhotic portal hypertension.
@en
type
label
Recurrent recessive mutation i ...... cirrhotic portal hypertension.
@en
prefLabel
Recurrent recessive mutation i ...... cirrhotic portal hypertension.
@en
P2093
P2860
P356
P1433
P1476
Recurrent recessive mutation i ...... cirrhotic portal hypertension.
@en
P2093
Amy L Stiegler
Buket Dalgic
Dhanpat Jain
Gulen Akyol
Güldal Yilmaz
Murat Günel
Richard P Lifton
Sinan Sari
Sílvia Vilarinho
Titus J Boggon
P2860
P304
P356
10.1002/HEP.28499
P407
P577
2016-02-13T00:00:00Z