Ushbu ishga iqtibos qilgan ishlar

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Ish: Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy

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2. The organic anion transporter SLCO2A1 constitutes the core component of the Maxi‐Cl channel

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3. The ATP-Releasing Maxi-Cl Channel: Its Identity, Molecular Partners, and Physiological/Pathophysiological Implications

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4. Pachydermoperiostosis Masquerading as Acromegaly

   М.М. Карімова, Zamira Halimova, Yulduz Urmanova +3

   MaqolaOAOchiq kirishHypertrophic osteoarthropathy and related conditionsJournal of the Endocrine Society20170 iqtibos

   ABIABI:AkademIndex/2017.article.000247