|
Volumn 19, Issue 11, 2004, Pages 2928-2929
|
Severe bladder dysfunction in a family with ADH receptor gene mutation responsible for X-linked nephrogenic diabetes insipidus [4]
|
Author keywords
[No Author keywords available]
|
Indexed keywords
AQUAPORIN 2;
VASOPRESSIN RECEPTOR;
ADOLESCENT;
ADULT;
BLADDER CAPACITY;
BLADDER DYSFUNCTION;
CASE REPORT;
CYSTOGRAPHY;
DISEASE ASSOCIATION;
DISEASE SEVERITY;
FAMILY;
GENE MUTATION;
GENETIC CODE;
HUMAN;
HYDROURETER;
INTERMITTENT CATHETERIZATION;
KIDNEY CONCENTRATING CAPACITY;
LETTER;
MALE;
NEPHROGENIC DIABETES INSIPIDUS;
PRIORITY JOURNAL;
SCHOOL CHILD;
URINALYSIS;
URINE VOLUME;
ADOLESCENT;
ADULT;
AQUAPORIN 2;
AQUAPORINS;
CHILD;
DIABETES INSIPIDUS, NEPHROGENIC;
GENETIC DISEASES, X-LINKED;
HUMANS;
MALE;
MUTATION;
RECEPTORS, VASOPRESSIN;
URINARY BLADDER;
URINARY BLADDER, NEUROGENIC;
|
EID: 8344223717
PISSN: 09310509
EISSN: None
Source Type: Journal
DOI: 10.1096/ndt/gfh486 Document Type: Letter |
Times cited : (22)
|
References (5)
|