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Tyni T, Kivela T, Lappi M, Summanen P, Nikoskelainen E, Pihko H: Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy
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Footnotes Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication
Radne nedjelje u srpnju: sve Radne nedjelje u kolovozu: sve Radne nedjelje u rujnu: 6., 13
The prevalence of Peyronies disease: results of a large survey
