Wolfram syndrome: Identification of a phenotypic and genotypic variant from Jordan

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 115, Issue 1, 2002, Pages 61-65

  Ajlouni, Kamel ^a,b   Jarrah, Nadim ^b   El Khateeb, Mohammed ^b   El Zaheri, Mohamed ^b   El Shanti, Hatem ^b,c   Lidral, Andrew ^d  

^a National Center for Diabetes Endocrinology and Genetics Jordan   (Jordan)

^b UNIVERSITY OF JORDAN   (Jordan)

^c JORDAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Jordan)

^d OHIO STATE UNIVERSITY   (United States)

Author keywords

Bleeding tendency; Diabetes mellitus; Peptic ulcer disease; Wolfram syndrome

Indexed keywords

ADOLESCENT; ADULT; ATAXIA; AUTOSOMAL RECESSIVE DISORDER; BLEEDING; CHROMOSOME 4P; CLINICAL ARTICLE; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; DIABETES INSIPIDUS; GENE LOCUS; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GENOTYPE; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; JORDAN; MENTAL DISEASE; OPTIC NERVE ATROPHY; PEPTIC ULCER; PERCEPTION DEAFNESS; PERIPHERAL NEUROPATHY; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SCHOOL CHILD; THROMBOCYTE AGGREGATION; WOLFRAM SYNDROME; ARTICLE; CHILD; CHROMOSOME 4; CHROMOSOME MAP; GENETICS; PATHOLOGY; URINARY TRACT DISEASE;

ADOLESCENT; ADULT; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 4; GENOTYPE; HUMAN; JORDAN; PEPTIC ULCER; PHENOTYPE; UROLOGIC DISEASES; VARIATION (GENETICS); WOLFRAM SYNDROME; HUMANS;

ATAXIA;

EID: 0036072103     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10345     Document Type: Review

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