Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1-Reference-Cited by-同舟云学术

Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1

Published:1999-11 Issue:5 Volume:65 Page:1279-1290
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Hardy Carol,Khanim Farhat,Torres Rosarelis,Scott-Brown Martin,Seller Anneke,Poulton Joanna,Collier David,Kirk Jeremy,Polymeropoulos Mihael,Latif Farida,Barrett Timothy

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome;Barrett;Lancet,1995

2. Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion;Barrientos;Am J Hum Genet,1996

3. A locus for bipolar affective disorder on chromosome 4p;Blackwood;Nat Genet,1996

4. Wolfram's syndrome: a clinical, diagnostic, and interpretive contribution;Blasi;Diabetes Care,1986

5. Mitochondrial abnormalites in the DIDMOAD syndrome;Bundey;J Inher Metab Dis,1992

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