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- Krankheit (de)
- maladie (fr)
- մարդու հիվանդություն (hy)
- хвороба людини (uk)
- Human disease (en)
- مرض يصيب الإنسان (ar)
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- A model of transport mechanisms in the distal convoluted tubule. Sodium chloride enters the cell via the apical thiazide-sensitive NCC and leaves the cell through the basolateral Cl− channel , and the Na+/K+-ATPase. Indicated also are the recently identified magnesium channel TRPM6 in the apical membrane, and a putative Na/Mg exchanger in the basolateral membrane. These transport mechanisms play a role in familial hypokalemia-hypomagnesemia or Gitelman syndrome. (en)
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- Mutations in SLC12A3, CLCKNB, MT-TI, MT-TF (en)
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- (en)
- + (en)
- N25.8 (en)
- E83.4 (en)
- E87.6 (en)
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- Primary renal tubular hypokalemic hypomagnesemia with hypocalciuria (en)
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- Gitelman syndrome (en)
- متلازمة غيتلمان (ar)
- Gitelman-Syndrom (de)
- Síndrome de Gitelman (es)
- Syndrome de Gitelman (fr)
- 지텔만 증후군 (ko)
- ギテルマン症候群 (ja)
- Zespół Gitelmana (pl)
- Syndroom van Gitelman (nl)
- Síndrome de Gitelman (pt)
- 吉特曼氏綜合症 (zh)
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