Clinically symptomatic heterozygous carnitine palmitoyltransferase II (CPT II) deficiency

Keyphrases

• Carnitine Palmitoyltransferase II Deficiency 100%
• Exon 66%
• Heterozygote 66%
• Rhabdomyolysis 66%
• Autosomal Recessive 33%
• Young Female 33%
• Young Males 33%
• Fever 33%
• Exercise-induced 33%
• Burning Sensation 33%
• Insolation 33%
• Paresis 33%
• Tennis Players 33%
• Triton X-100 (TX-100) 33%
• Marathon Runners 33%
• Muscle Pain 33%
• Amateur 33%
• Malonyl-CoA 33%
• Muscle Cramps 33%
• Professional Tennis 33%
• Myalgia 33%
• Proximal Weakness 33%
• Female Professionals 33%
• CPT2 Gene 33%
• Symptomatic Patients 33%

Biochemistry, Genetics and Molecular Biology

• Carnitine Palmitoyltransferase II Deficiency 100%
• Exon 66%
• Autosomal Recessive Disorder 33%
• Genetic Carrier 33%
• Allele 33%
• Intron 33%
• Sensation 33%
• Heterozygote 33%
• Homogenate 33%
• Malonyl-CoA 33%
• Isoprenaline 33%