<p>Domestic cats genotyped for the <i>CLCN1</i> mutation associated with myotonia congenita.</p
<p>* Chartreux (n = 21), Sphynx (n = 20), British SH and LH (n = 20), Norwegian Forest Cat (n = 20),...
*<p>All available affected cats were used in GWAS except only four of nine cats in the pedigree (<a ...
The domestic cat (Felis catus) numbers over 94 million in the USA alone, occupies households as a co...
<p>SNPs analyses of <i>CLCN1</i> in cats with and without myotonia congenita.</p
<div><p>Myotonia congenita (MC) is a skeletal muscle channelopathy characterized by inability of the...
Myotonia congenita (MC) is a skeletal muscle channelopathy characterized by inability of the muscle ...
Abstract Case Description A 10‐month‐old castrated male domestic longhair cat was evaluated for incr...
<p>a. Genomic sequence of three control cats and the five affected cats. The red rectangle indicates...
Observed CMAH gene variants (nsSNVs and indels), PROVEAN analyses, genotypes, and haplotypes in diff...
State-of-the-art health care includes genome sequencing of the patient to identify genetic variants ...
State-of-the-art health care includes genome sequencing of the patient to identify genetic variants ...
State-of-the-art health care includes genome sequencing of the patient to identify genetic variants ...
Chantier qualité GAInternational audienceObjectives: The MYBPC3-A31P mutation has been identified in...
OBJECTIVES: A missense mutation (A31P) in the cardiac myosin binding protein C gene has been associa...
The release of new DNA-based diagnostic tools has increased tremendously in companion animals. Over ...
<p>* Chartreux (n = 21), Sphynx (n = 20), British SH and LH (n = 20), Norwegian Forest Cat (n = 20),...
*<p>All available affected cats were used in GWAS except only four of nine cats in the pedigree (<a ...
The domestic cat (Felis catus) numbers over 94 million in the USA alone, occupies households as a co...
<p>SNPs analyses of <i>CLCN1</i> in cats with and without myotonia congenita.</p
<div><p>Myotonia congenita (MC) is a skeletal muscle channelopathy characterized by inability of the...
Myotonia congenita (MC) is a skeletal muscle channelopathy characterized by inability of the muscle ...
Abstract Case Description A 10‐month‐old castrated male domestic longhair cat was evaluated for incr...
<p>a. Genomic sequence of three control cats and the five affected cats. The red rectangle indicates...
Observed CMAH gene variants (nsSNVs and indels), PROVEAN analyses, genotypes, and haplotypes in diff...
State-of-the-art health care includes genome sequencing of the patient to identify genetic variants ...
State-of-the-art health care includes genome sequencing of the patient to identify genetic variants ...
State-of-the-art health care includes genome sequencing of the patient to identify genetic variants ...
Chantier qualité GAInternational audienceObjectives: The MYBPC3-A31P mutation has been identified in...
OBJECTIVES: A missense mutation (A31P) in the cardiac myosin binding protein C gene has been associa...
The release of new DNA-based diagnostic tools has increased tremendously in companion animals. Over ...
<p>* Chartreux (n = 21), Sphynx (n = 20), British SH and LH (n = 20), Norwegian Forest Cat (n = 20),...
*<p>All available affected cats were used in GWAS except only four of nine cats in the pedigree (<a ...
The domestic cat (Felis catus) numbers over 94 million in the USA alone, occupies households as a co...
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