Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.

Wolfram syndrome (DIDMOAD syndrome; MIM 222300) is an autosomal recessive neurodegenerative disorder characterized by juvenile-onset diabetes mellitus and bilateral optic atrophy. Previous linkage analysis of multiply affected families indicated that the gene for Wolfram syndrome is on chromosome 4p...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Collier, D. A., Barrett, T. G., Curtis, D., Macleod, A., Arranz, M. J., Maassen, J. A., Bundey, S.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1996
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1914816/
https://ncbi.nlm.nih.gov/pubmed/8808601
Etiketak: Etiketa erantsi
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