a<p>ΔG at 426 corresponds to a −1 bp deletion within G<sup>5</sup>SSR<sub>426</sub>; ΔC at 362 corresponds to a −1 bp deletion within a mononucleotide SSR of four Cs from 362 to 365 (C<sup>4</sup>SSR<sub>362</sub>); ΔC at 431 corresponds to a −1 bp deletion within C<sup>6</sup>SSR<sub>431</sub>. “None” refers to conversion to mucoidy occurring in the absence of <i>mucA</i> mutations. The nature of these non-<i>mucA</i> alterations leading to a mucoid phenotype was not investigated in this work.</p>b<p>Stop codon produced at the site of the mutation by substitutions or placed in frame by frameshift mutations.</p
The mutation R403stop was found in an individual with mut(0) methylmalonic aciduria (MMA) which resu...
Mucopolysaccharidosis (MPS) types IIIA, B, C, and D are a group of autosomal recessive lysosomal sto...
Isolated methylmalonic aciduria (MMA) is an autosomal-recessive disorder of propionate metabolism th...
<p>A fragment of the <i>P. aeruginosa mucA</i> gene where the site directed mutagenesis was performe...
Murine mucopolysaccharidosis type VII is a heritable disease caused by a spontaneous mutation, gus(m...
In Pseudomonas aeruginosa, conversion to the mucoid phenotype marks the onset of an irreversible sta...
Mutations and the changes determined in the sequence of mucA in mucoid (M) and non-mucoid (NM) P. ae...
a<p>SNP and indel mutations were considered.</p>b<p>Clusters were defined according to maximum-parsi...
Inducible mutagenesis in Escherichia coli requires the direct action of the chromosomally encoded Um...
Alginate biosynthesis in Pseudomonas aeruginosa is a highly regulated process in which algU and mucA...
a<p>For each study, only the isolates for which the <i>mucA</i> mutations were reported were conside...
Genetic complementation of fibroblasts from patients with methylmalonic aciduria (MMA) defines a uni...
The mutation R403stop was found in an individual with mut(0) methylmalonic aciduria (MMA) which resu...
AbstractThe present study aimed to characterize mutant alleles in Mucopolysaccharidosis II and evalu...
The mut' mutation resulting in methylmalonyl CoA mutase (MCM) apoenzyme deficiency and methylmalonic...
The mutation R403stop was found in an individual with mut(0) methylmalonic aciduria (MMA) which resu...
Mucopolysaccharidosis (MPS) types IIIA, B, C, and D are a group of autosomal recessive lysosomal sto...
Isolated methylmalonic aciduria (MMA) is an autosomal-recessive disorder of propionate metabolism th...
<p>A fragment of the <i>P. aeruginosa mucA</i> gene where the site directed mutagenesis was performe...
Murine mucopolysaccharidosis type VII is a heritable disease caused by a spontaneous mutation, gus(m...
In Pseudomonas aeruginosa, conversion to the mucoid phenotype marks the onset of an irreversible sta...
Mutations and the changes determined in the sequence of mucA in mucoid (M) and non-mucoid (NM) P. ae...
a<p>SNP and indel mutations were considered.</p>b<p>Clusters were defined according to maximum-parsi...
Inducible mutagenesis in Escherichia coli requires the direct action of the chromosomally encoded Um...
Alginate biosynthesis in Pseudomonas aeruginosa is a highly regulated process in which algU and mucA...
a<p>For each study, only the isolates for which the <i>mucA</i> mutations were reported were conside...
Genetic complementation of fibroblasts from patients with methylmalonic aciduria (MMA) defines a uni...
The mutation R403stop was found in an individual with mut(0) methylmalonic aciduria (MMA) which resu...
AbstractThe present study aimed to characterize mutant alleles in Mucopolysaccharidosis II and evalu...
The mut' mutation resulting in methylmalonyl CoA mutase (MCM) apoenzyme deficiency and methylmalonic...
The mutation R403stop was found in an individual with mut(0) methylmalonic aciduria (MMA) which resu...
Mucopolysaccharidosis (MPS) types IIIA, B, C, and D are a group of autosomal recessive lysosomal sto...
Isolated methylmalonic aciduria (MMA) is an autosomal-recessive disorder of propionate metabolism th...