Wolfram syndrome - clinical and diagnostic details.

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Wolfram syndrome - clinical and diagnostic details.

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2009 nî lūn-bûn

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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2009年學術文章

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2009年學術文章

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Wolfram syndrome - clinical and diagnostic details.

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Wolfram syndrome - clinical and diagnostic details.

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Wolfram syndrome - clinical and diagnostic details.

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Wolfram syndrome - clinical and diagnostic details.

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Wolfram syndrome - clinical and diagnostic details.

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Wolfram syndrome - clinical and diagnostic details.

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P1476

Wolfram syndrome - clinical and diagnostic details.

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P2093

Hazel Gonsalves

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Maneesh Mailankot

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Navin Mulamani

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Rohith Valsalan

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Shubha Sheshadri

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P2860

Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium

Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1

Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.

The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells.

Wolfram syndrome: evidence of a diffuse neurodegenerative disease by magnetic resonance imaging.

Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene product.

Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.

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s12291-009-0079-x

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436-438

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scholarly article

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10.1007/S12291-009-0079-X

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P478

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2009-10-01T00:00:00Z

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232722269

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23105875

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3453061

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