Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss.
Nephrol Dial Transplant
; 18(3): 512-6, 2003 Mar.
Article
in En
| MEDLINE
| ID: mdl-12584272
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Receptors, Drug
/
Carrier Proteins
/
Sodium-Potassium-Exchanging ATPase
/
Symporters
/
Kidney Diseases
/
Magnesium
/
Membrane Proteins
/
Mutation
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Nephrol Dial Transplant
Journal subject:
NEFROLOGIA
/
TRANSPLANTE
Year:
2003
Document type:
Article
Affiliation country:
Netherlands
Country of publication:
United kingdom