The clinical, biochemical, and molecular spectrum of ornithine transcarbamylase deficiency.
about
Suggested guidelines for the diagnosis and management of urea cycle disordersSeizures and X-linked intellectual disabilityOrthotopic liver transplantation for ornithine transcarbamylase deficiency with hyperammonemic encephalopathy.Ornithine transcarbamylase deficiency combined with type 1 diabetes mellitus - a challenge in clinical and dietary management.Cross-sectional observational study of 208 patients with non-classical urea cycle disorders
P2860
The clinical, biochemical, and molecular spectrum of ornithine transcarbamylase deficiency.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
The clinical, biochemical, and ...... e transcarbamylase deficiency.
@ast
The clinical, biochemical, and ...... e transcarbamylase deficiency.
@en
type
label
The clinical, biochemical, and ...... e transcarbamylase deficiency.
@ast
The clinical, biochemical, and ...... e transcarbamylase deficiency.
@en
prefLabel
The clinical, biochemical, and ...... e transcarbamylase deficiency.
@ast
The clinical, biochemical, and ...... e transcarbamylase deficiency.
@en
P1476
The clinical, biochemical, and ...... e transcarbamylase deficiency.
@en
P2093
P304
P577
1992-12-01T00:00:00Z