Molecular Characterization of WFS1 in Patients with Wolfram Syndrome

Wolfram (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness) syndrome is a rare autosomal-recessive neurodegenerative disorder that is characterized by juvenile-onset diabetes mellitus, optic atrophy, diabetes insipidus, and sensorineural hearing impairment. A gene responsible for Wo...

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Autori principali: Van Den Ouweland, Johannes M. W., Cryns, Kim, Pennings, Ronald J. E., Walraven, Inge, Janssen, George M. C., Maassen, J. Antonie, Veldhuijzen, Bernard F. E., Arntzenius, Alexander B., Lindhout, Dick, Cremers, Cor W. R. J., Van Camp, Guy, Dikkeschei, Lambert D.
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Investigative Pathology 2003
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Regular Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1907324/
https://ncbi.nlm.nih.gov/pubmed/12707373
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