Nalaganje...

Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC): Compound heterozygous mutation in the claudin 16 (CLDN16) gene

BACKGROUND: Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC) is an autosomal recessive disorder of renal calcium and magnesium wasting frequently complicated by progressive chronic renal failure in childhood or adolescence. METHODS: A 7 year old boy was investigated followin...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: Hampson, Geeta, Konrad, Martin A, Scoble, John
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2008
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2562370/
https://ncbi.nlm.nih.gov/pubmed/18816383
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2369-9-12
Oznake: Označite
Brez oznak, prvi označite!