Author:
Trijbels F.,Sengers R.,Monnens L.,Janssen A.,Willems J.,Ter Laak H.,Stadhouders A.
Subject
Genetics (clinical),Genetics
Reference5 articles.
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3. Monnens, L., Gabreëls, F. and Willems, J. A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness.J. Pediatr. 86 (1975) 983
4. Van Biervliet, J. P. G. M., Bruinvis, L., Ketting, D., De Bree, P. K., Van der Heiden, C., Wadman, S. K., Willems, J. L., Bookelman, H., Van Haelst, U. J. G. and Monnens, L. A. H. Hereditary mitochondrial myopathy with lactic acidemia, a de Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles.Pediatr. Res. 11 (1977) 1088–1093
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