<p>Mutations which are classified as definitely pathogenic in humans that are found to be fixed in other species.</p
<p>Mutations in the gene segments of the six whole genomes of H1N1pdm Indian isolates with respect t...
a<p>These mutationsare considered pathogenic because they could produce alterations in the splicing ...
<p>Classification of <i>msh4/5</i> mutations that affect protein stability or interaction with DNA.<...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
<p>Clinical Characteristics and Detected Deleterious Mutations in Each Patient Pair.</p
<p>Pathogenic genetic variants identified in affected individuals with overlapping syndromes.</p
<p>doi:10.1371/journal.pone.0078496.t001</p><p>Causative mutations and putatively pathogenic variant...
<p>Specific mutations within each clade are indicated. Fixed mutations, systematically present in al...
<p>Mutations identified in <i>M</i>. <i>tuberculosis</i> genome and their frequency.</p
Genes having mutations, which were assessed as a high or moderate impact and confirmed in the COSMIC...
<p>Mutations in the gene segments of the six whole genomes of H1N1pdm Indian isolates with respect t...
a<p>These mutationsare considered pathogenic because they could produce alterations in the splicing ...
<p>Classification of <i>msh4/5</i> mutations that affect protein stability or interaction with DNA.<...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
Mutations in human genetic disease include single base-pair substitutions in coding, regulatory and ...
<p>Clinical Characteristics and Detected Deleterious Mutations in Each Patient Pair.</p
<p>Pathogenic genetic variants identified in affected individuals with overlapping syndromes.</p
<p>doi:10.1371/journal.pone.0078496.t001</p><p>Causative mutations and putatively pathogenic variant...
<p>Specific mutations within each clade are indicated. Fixed mutations, systematically present in al...
<p>Mutations identified in <i>M</i>. <i>tuberculosis</i> genome and their frequency.</p
Genes having mutations, which were assessed as a high or moderate impact and confirmed in the COSMIC...
<p>Mutations in the gene segments of the six whole genomes of H1N1pdm Indian isolates with respect t...
a<p>These mutationsare considered pathogenic because they could produce alterations in the splicing ...
<p>Classification of <i>msh4/5</i> mutations that affect protein stability or interaction with DNA.<...
DOI
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