Genotype–phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle α-actin
Carina Wallgren‐Pettersson(University of Helsinki), Nigel G. Laing(Harry Perkins Institute of Medical Research), Norma B. Romero(Inserm), Alan H. Beggs(Boston Children's Hospital), Hans H. Goebel(University Medical Center of the Johannes Gutenberg University Mainz), Katarina Pelin(University of Helsinki), Francesco Muntoni(Great Ormond Street Hospital), Kathryn N. North(The University of Melbourne)
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