WS1 gene mutation analysis of wolfram syndrome in a Chinese patient and a systematic review of literatures

Endocrine

Volumn 38, Issue 2, 2010, Pages 147-152

  Yu, Guang ^a   Yu, Man Li ^a   Wang, Jia Feng ^a   Gao, Cong Rong ^a   Chen, Zhong Jin ^b  

^a SECOND MILITARY MEDICAL UNIVERSITY   (China)

^b FUDAN UNIVERSITY   (China)

Author keywords

DIDMOAD; Genetic diagnosis; Mutation; WFS1 gene; Wolfram syndrome

Indexed keywords

DESMOPRESSIN; INSULIN;

ADOLESCENT; ADULT; ARTICLE; BLADDER IRRITATION; CASE REPORT; CATARACT; CHINESE; COMPUTER ASSISTED TOMOGRAPHY; CYSTOSTOMY; DIABETES INSIPIDUS; DIURESIS; ECHOGRAPHY; FLUID THERAPY; GENE; GENE MUTATION; GENE SEQUENCE; HEMODIALYSIS; HUMAN; HYPERGLYCEMIA; INSULIN DEPENDENT DIABETES MELLITUS; KIDNEY DISEASE; MALE; MENTAL DISEASE; MUTATIONAL ANALYSIS; NONSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; NYSTAGMUS; OPEN READING FRAME; POLYDIPSIA; PRIORITY JOURNAL; URODYNAMICS; WATER DEPRIVATION; WOLFRAM SYNDROME; WS1 GENE;

EID: 78149416080     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-010-9350-4     Document Type: Article

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