Five Novel Mutations in ARG1 Gene in Chinese Patients of Argininemia

Author:

Wu Tong-Fei,Liu Yu-Peng,Li Xi-Yuan,Wang Qiao,Ding Yuan,Ma Yan-Yan,Song Jin-Qing,Yang Yan-Ling

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference28 articles.

1. Clinical features and neurologic progression of hyperargininemia;Carvalho;Pediatr Neurol,2012

2. Familial hyperargininaemia;Terheggen;Arch Dis Child,1975

3. Late diagnosis of congenital argininemia during administration of sodium valproate;Christmann;Rev Neurol (Paris),1990

4. Arginase deficiency in multiple tissues in argininemia;Michels;Clin Genet,1978

5. Argininemia presenting with progressive spastic diplegia;Lee;Pediatr Neurol,2011

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