Leila Scholle

Naturwissenschaftlerin

Born: 1978, Teheran

Has participated in:

Biochemische Charakterisierung mitochondrialer Myopathien in Trägern der m.3243A>G Mutation und Patienten mit Carnitin-Palmitoyltransferase II-Mangel : kumulative Schrift
Camptocormia as a novel phenotype in a heterozygous POLG2 mutation
Palmitate but not oleate exerts a negative effect on oxygen utilization in myoblasts of patients with the m.3243A>G mutation: a pilot study
Myalgia in 30 Patients with Suspected Myopathy

All Objects (7)

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Leila Scholle

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