Full text
PDF![553](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cb/1672681/81137ea53d14/brmedj01436-0029.png)
![554](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cb/1672681/72734703f71f/brmedj01436-0030.png)
![555](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cb/1672681/6ae11adebfe6/brmedj01436-0031.png)
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- DiMauro S., DiMauro P. M. Muscle carnitine palmityltransferase deficiency and myoglobinuria. Science. 1973 Nov 20;182(4115):929–931. doi: 10.1126/science.182.4115.929. [DOI] [PubMed] [Google Scholar]
- Engel A. G., Angelini C. Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome. Science. 1973 Mar 2;179(4076):899–902. doi: 10.1126/science.179.4076.899. [DOI] [PubMed] [Google Scholar]
- JORDANS G. H. The familial occurrence of fat containing vacuoles in the leukocytes diagnosed in two brothers suffering from dystrophia musculorum progressiva (ERB.). Acta Med Scand. 1953;145(6):419–423. doi: 10.1111/j.0954-6820.1953.tb07038.x. [DOI] [PubMed] [Google Scholar]
- Rozenszajn L., Klajman A., Yaffe D., Efrati P. Jordans' anomaly in white blood cells. Report of case. Blood. 1966 Aug;28(2):258–265. [PubMed] [Google Scholar]