Primary coenzyme Q10 Deficiency-6 (COQ10D6): Two siblings with variable expressivity of the renal phenotype
| Autor: | Yuruk Yildirim, Zeynep a, ∗, Toksoy, Guven b, Uyguner, Oya b, Nayir, Ahmet a, Yavuz, Sevgi c, Altunoglu, Umut b, Turkkan, Ozde Nisa a, Sevinc, Burcu b, Gokcay, Gulden d, Kurkcu Gunes, Dilek d, Kiyak, Aysel c, Yilmaz, Alev a |
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| Zdroj: | In European Journal of Medical Genetics January 2020 63(1) |
| Databáze: | ScienceDirect |
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