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Leucopternis princeps voucher LSUMNS B-11751 ATP synthase F0 subunit 8 (ATP8) and ATP synthase F0 subunit 6 (ATP6) genes, complete cds; mitochondrial

GenBank: DQ148387.1

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  • Leucopternis princeps voucher LSUMNS B-11751 ATP synthase F0 subunit 8 (ATP8) an...
    Leucopternis princeps voucher LSUMNS B-11751 ATP synthase F0 subunit 8 (ATP8) and ATP synthase F0 subunit 6 (ATP6) genes, complete cds; mitochondrial
    gi|76009186|gb|DQ148387.1|
    Nucleotide
  • Bartter Syndrome
    Bartter Syndrome
    A group of disorders caused by defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA; HYPERCALCIURIA; metabolic A...<br/>Year introduced: 2005 (1975)
    MeSH
  • Solute Carrier Family 12
    Solute Carrier Family 12
    Inorganic cation-chloride cotransporters mediating the movement of inorganic SODIUM and/or POTASSIUM cations, coupled to the movement of CHLORIDE anions. The solute carrier 12...<br/>Year introduced: 2024
    MeSH

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