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Whole-exome sequencing in Russian children with non-type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY-related and unrelated genes

The present study reports on the frequency and the spectrum of genetic variants causative of monogenic diabetes in Russian children with non-type 1 diabetes mellitus. The present study included 60 unrelated Russian children with non-type 1 diabetes mellitus diagnosed before the age of 18 years. Gene...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Med Rep
Prif Awduron: Glotov, Oleg S., Serebryakova, Elena A., Turkunova, Mariia E., Efimova, Olga A., Glotov, Andrey S., Barbitoff, Yury A., Nasykhova, Yulia A., Predeus, Alexander V., Polev, Dmitrii E., Fedyakov, Mikhail A., Polyakova, Irina V., Ivashchenko, Tatyana E., Shved, Natalia Y., Shabanova, Elena S., Tiselko, Alena V., Romanova, Olga V., Sarana, Andrey M., Pendina, Anna A., Scherbak, Sergey G., Musina, Ekaterina V., Petrovskaia-Kaminskaia, Anastasiia V., Lonishin, Liubov R., Ditkovskaya, Liliya V., Zhelenina, Liudmila A., Tyrtova, Ludmila V., Berseneva, Olga S., Skitchenko, Rostislav K., Suspitsin, Evgenii N., Bashnina, Elena B., Baranov, Vladislav S.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: D.A. Spandidos 2019
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6854535/
https://ncbi.nlm.nih.gov/pubmed/31638168
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2019.10751
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