AbstractWe determined the DNA sequence of the adenylosuccinate lyase (ASL) gene from a 13 year-old female, who showed a reduced ASL enzymatic activity in lymphocytes and red blood cells and suffered from severe psychomotor retardation. The patient was the offspring of a non-consanguineous marriage. She was found to be compound heterozygous for two missense-mutations located on different alleles (C300–G and G1266–T): the first mutation replaces Pro75 by Ala, the second mutation replaces Asp397 by Tyr
We describe a previously healthy 14-year-old girl with acute onset autoimmune hemolytic anemia, asso...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
A deficiency of adenylosuccinate lyase (ASDL) is characterised by the accumulation of SAICAriboside ...
We have examined the molecular basis of three cases of severe mental retardation with autistic featu...
The deficiency of adenylosuccinate lyase (ADSL, also termed adenylosuccinase) is an autosomal recess...
Pathogenic variants in the argininosuccinate lyase (ASL) gene have been shown to cause argininosucci...
An Australian patient with autism was found to be heterozygous for two mutations in the gene encodin...
AbstractWe studied the effect of trans-4-hydroxy-2-nonenal on the wild-type human adenylosuccinate l...
Argininosuccinate lyase deficiency (ASLD) is caused by a defect of the urea cycle enzyme argininosuc...
Most cases of adenylosuccinate lyase (ADSL OMIM 103050) deficiency reported to date are confined to ...
Adenylosuccinate lyase (ADSL; also called “adenylosuccinase”) catalyzes two steps in the synthesis o...
BackgroundAdenylosuccinate lyase deficiency (ADSLD) is an ultrarare neurometabolic recessive disorde...
Argininosuccinic aciduria (ASAuria) is an inborn error of metabolism caused by mutations in the argi...
We report on the striking variable expression of adenylosuccinate lyase (ADSL) deficiency in three p...
Argininosuccinic aciduria (ASA) is an autosomal recessive urea cycle disorder caused by deficiency o...
We describe a previously healthy 14-year-old girl with acute onset autoimmune hemolytic anemia, asso...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
A deficiency of adenylosuccinate lyase (ASDL) is characterised by the accumulation of SAICAriboside ...
We have examined the molecular basis of three cases of severe mental retardation with autistic featu...
The deficiency of adenylosuccinate lyase (ADSL, also termed adenylosuccinase) is an autosomal recess...
Pathogenic variants in the argininosuccinate lyase (ASL) gene have been shown to cause argininosucci...
An Australian patient with autism was found to be heterozygous for two mutations in the gene encodin...
AbstractWe studied the effect of trans-4-hydroxy-2-nonenal on the wild-type human adenylosuccinate l...
Argininosuccinate lyase deficiency (ASLD) is caused by a defect of the urea cycle enzyme argininosuc...
Most cases of adenylosuccinate lyase (ADSL OMIM 103050) deficiency reported to date are confined to ...
Adenylosuccinate lyase (ADSL; also called “adenylosuccinase”) catalyzes two steps in the synthesis o...
BackgroundAdenylosuccinate lyase deficiency (ADSLD) is an ultrarare neurometabolic recessive disorde...
Argininosuccinic aciduria (ASAuria) is an inborn error of metabolism caused by mutations in the argi...
We report on the striking variable expression of adenylosuccinate lyase (ADSL) deficiency in three p...
Argininosuccinic aciduria (ASA) is an autosomal recessive urea cycle disorder caused by deficiency o...
We describe a previously healthy 14-year-old girl with acute onset autoimmune hemolytic anemia, asso...
Loss of function of the urea cycle enzyme argininosuccinate lyase (ASL) is caused by mutations in th...
A deficiency of adenylosuccinate lyase (ASDL) is characterised by the accumulation of SAICAriboside ...