Novel complex Re-Arrangement of ARG1 commonly shared by unrelated patients with Hyperargininemia-Reference-Cited by-同舟云学术

Novel complex Re-Arrangement of ARG1 commonly shared by unrelated patients with Hyperargininemia

Published:2014-01 Issue:1 Volume:533 Page:240-245
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Mohseni Jafar,Boon Hock Chia,Abdul Razak Che,Othman Syah Nor Iman,Hayati Fatemeh,PeiTee Winnie Ong,Haniffa Muzhirah,Zilfalil Bin Alwi,Mohd. Rawi Rowani,Ngu Lock-Hock,Sasongko Teguh Haryo

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference21 articles.

1. Identification of a Novel R21X Mutation in the Liver Type Arginase Gene (ARG1) in Four Portuguese Patients with Argininemia;Cardoso;Hum. Mutat.,1999

2. Analysis of novel ARG1 mutations causing hyperargininemia and correlation with arginase I activity in erythrocytes;Carvalho;Gene,2012

3. Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma;Cowell;Eur. J. Hum. Genet.,1994

4. Exome Variant Server, NHLBI GO Exome Sequencing Project (ESP), Seattle, WA (URL: http://evs.gs.washington.edu/EVS/) [Accessed on 19 August 2013].

5. Molecular genetic study of human arginase deficiency;Grody;Am. J. Hum. Genet.,1992

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