FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic studyAnu Suomalainen, Henna Tyynismaa, Ksenia Sevastianova et al.|The Lancet Neurology|2011Cited by 420
Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in<i>TPM2</i>and<i>TPM3</i>Causing Congenital MyopathiesM. Marttila, Carina Wallgren‐Pettersson, Vilma‐Lotta Lehtokari et al.|Human Mutation|2014Cited by 111