Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Y. Seyedena"'
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 39, Iss 6, Pp 725-730 (2006)
Leber's hereditary optic neuropathy (LHON) is a maternally inherited form of retinal ganglion cell degeneration leading to optic atrophy in young adults. Several mutations in different genes can cause LHON (heterogeneity). The ND6 gene is one of the
Externí odkaz:
https://doaj.org/article/20fef4dd8de54b8e93dbbe943986a9a4
Publikováno v:
Bratislavske lekarske listy. 120(8)
OBJECTIVES The aim of this study was to evaluate the possible association of miR-206 serum as an indicator of diagnosis in patients with coronary artery disease. METHODS In this study, 100 patients with coronary artery disease who had angiography and
Publikováno v:
Brazilian Journal of Medical and Biological Research, Volume: 39, Issue: 6, Pages: 725-730, Published: JUN 2006
Brazilian Journal of Medical and Biological Research v.39 n.6 2006
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Vol 39, Iss 6, Pp 725-730 (2006)
Brazilian Journal of Medical and Biological Research v.39 n.6 2006
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Vol 39, Iss 6, Pp 725-730 (2006)
Leber's hereditary optic neuropathy (LHON) is a maternally inherited form of retinal ganglion cell degeneration leading to optic atrophy in young adults. Several mutations in different genes can cause LHON (heterogeneity). The ND6 gene is one of the
Publikováno v:
Bratislava Medical Journal / Bratislavské Lekárske Listy; Aug2019, Vol. 120 Issue 8, p581-585, 5p
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