Magnhild Rasmussen
- Succinate‐CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients
2015/10/16 by Rosalba Carrozzo, Daniela Verrigni, Magnhild Rasmussen +31 · 1 citation
Biochemistry, Genetics and Molecular Biology · Neuroscience · Medicine · #Genomics and Rare Diseases #Metabolism and Genetic Disorders #Neurological diseases and metabolism #Genotype #Phenotype #Human genetics #Genetics #DNA ligase #Medicine #Biology #Internal medicine #Gene