*<p>Nucleotide numbers refer to genomic DNA and are numbered from the transcription start site. Amino acid replacement mutations are indicated according to codon number; The reference sequence is available on the NCBI (GenBank accession number: NM_003880.3).</p
Boning up on mutations: assessing the significance of candidate disease-causing DNA sequence variati...
<p>Nucleotide numbering for cDNA –based nomenclature uses 1+ as to the A of the ATG translation init...
<p>Mutation nomenclature follows the recommended guidelines of the Human Genome Variation Society, w...
<p>The pedigrees and automated sequencing traces of the <i>WISP3</i> gene mutations in the two famil...
<p>The nucleotide mutations, corresponding amino acid changes and the frequency of occurrence of mut...
<p>Base mutation locations indicate mutated nucleotide numbering in the whole AP009048 reference gen...
<p>Positions of the nucleotide (nt) mutation and the correlating amino acid (aa) are presented based...
<p>Positions of the nucleotide (nt) mutation and the correlating amino acid (aa) are presented based...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
Page 1 contains the nucleotide substitutions observed on each evolved lineage. Page 2 contains a sc...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
This database consists of over 24 000 mutations in 18 viral, bacterial, yeast or mammalian genes. Th...
Introduction: Progressive pseudorheumatoid dysplasia (PPD) is an autosomal recessive genetic disorde...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
Each mutation spectrum in this database is a dataset of changes in DNA base sequence in mutations in...
Boning up on mutations: assessing the significance of candidate disease-causing DNA sequence variati...
<p>Nucleotide numbering for cDNA –based nomenclature uses 1+ as to the A of the ATG translation init...
<p>Mutation nomenclature follows the recommended guidelines of the Human Genome Variation Society, w...
<p>The pedigrees and automated sequencing traces of the <i>WISP3</i> gene mutations in the two famil...
<p>The nucleotide mutations, corresponding amino acid changes and the frequency of occurrence of mut...
<p>Base mutation locations indicate mutated nucleotide numbering in the whole AP009048 reference gen...
<p>Positions of the nucleotide (nt) mutation and the correlating amino acid (aa) are presented based...
<p>Positions of the nucleotide (nt) mutation and the correlating amino acid (aa) are presented based...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
Page 1 contains the nucleotide substitutions observed on each evolved lineage. Page 2 contains a sc...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
This database consists of over 24 000 mutations in 18 viral, bacterial, yeast or mammalian genes. Th...
Introduction: Progressive pseudorheumatoid dysplasia (PPD) is an autosomal recessive genetic disorde...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
Each mutation spectrum in this database is a dataset of changes in DNA base sequence in mutations in...
Boning up on mutations: assessing the significance of candidate disease-causing DNA sequence variati...
<p>Nucleotide numbering for cDNA –based nomenclature uses 1+ as to the A of the ATG translation init...
<p>Mutation nomenclature follows the recommended guidelines of the Human Genome Variation Society, w...