Showing 1 - 7 results of 7 for search 'Ana Perdomo-Ramirez', query time: 0.07s Refine Results
  1. 1
    Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease
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    Article
  2. 2
    Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations
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    Article
  3. 3
    Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
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    Article
  4. 4
    Hereditary renal hypouricaemia type 1 and 2 in three Spanish children. Review of published paediatric cases
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    Article
  5. 5
    Hipouricemia renal hereditaria tipo 1 y 2 en tres niños españoles. Revisión de casos pediátricos publicados
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    Article
  6. 6
    Considerations about the molecular basis of some kidney tubule disorders in relation to inbreeding and population displacement
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    Article
  7. 7
    Consideraciones acerca de las bases moleculares de algunas tubulopatías en relación con la endogamia y los desplazamientos poblacionales
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    Article
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