ASS1 gene mutation in a neonate with citrullinemia type I

OBJECTIVE: To identify the genetic mutation in ASS1 gene in a Chinese family with citrullinemia typeI, which may provide a basis for the diagnosis and genetic counseling

Bibliographische Detailangaben
Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 52(2014), 10 vom: 01. Okt., Seite 788-91
1. Verfasser: Xie, Bobo (VerfasserIn)
Weitere Verfasser: Chen, Rongyu, Wang, Jin, Luo, Jingsi, Li, Wang, Chen, Shaoke
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:Journal Article Argininosuccinate Synthase EC 6.3.4.5
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245 1 0 |a ASS1 gene mutation in a neonate with citrullinemia type I 
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500 |a Citation Status MEDLINE 
520 |a OBJECTIVE: To identify the genetic mutation in ASS1 gene in a Chinese family with citrullinemia typeI, which may provide a basis for the diagnosis and genetic counseling 
520 |a METHOD: Genomic DNA was isolated from peripheral blood samples of the family members. Mutation analysis of ASS1 gene was carried out by PCR and Sanger sequencing. Biostructural analysis of the mutated ASS1 was completed by Phyre server 
520 |a RESULT: Double heterozygous mutations in the proband were identified: c.951delT (F317LfsX375) and c.1087C>T (R363W), which were confirmed in the proband's father and mother, respectively. It was found that the c.951delT mutation might change the formation of a dimer or a tetramer and the function of ASS1 protein 
520 |a CONCLUSION: Double heterozygous mutations for c.951delT and c.1087C>T have been found in a proband with citrullinemia typeI. The c.951delT is a novel mutation in citrullinemia typeI, which may change the configuration of ASS1 protein and result in ASS1 dysfunction 
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700 1 |a Chen, Rongyu  |e verfasserin  |4 aut 
700 1 |a Wang, Jin  |e verfasserin  |4 aut 
700 1 |a Luo, Jingsi  |e verfasserin  |4 aut 
700 1 |a Li, Wang  |e verfasserin  |4 aut 
700 1 |a Chen, Shaoke  |e verfasserin  |4 aut 
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