Add to ORKGWolfram syndrome patients are mainly characterised by juvenile onset diabetes mellitus and optic atrophy. A synonym is the acronym DIDMOAD: diabetes insipidus, diabetes mellitus, optic atrophy, deafness. Diabetes insipidus and sensorineural high-frequency hearing impairment are important additional features. This rare autosomal recessively inherited neurodegenerative syndrome is caused by mainly inactivating mutations in the WFS1 gene. It is located at chromosome 4p16 and encodes wolframin, a transmembrane protein. No function has yet been ascribed to this protein
Wolfram syndrome 1, a rare autosomal recessive neurodegenerative disease, is caused by mutations in ...
BACKGROUND: Wolfram Syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized...
Wolfram syndrome is a rare autosomal recessive disorder characterized by optic atrophy and diabetes ...
Item does not contain fulltextWolfram syndrome patients are mainly characterised by juvenile onset d...
Item does not contain fulltextWFS1 is a novel gene and encodes an 890 amino-acid glycoprotein (wolfr...
Wolfram (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness) syndrome is a rare auto...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed...
WFS1 is a novel gene and encodes an 890 amino-acid glycoprotein (wolframin), predominantly localized...
Item does not contain fulltextWolfram (diabetes insipidus, diabetes mellitus, optic atrophy, and dea...
OBJECTIVE\u2014 Wolfram syndrome is an autosomal recessive neurodegenerative disorder characterized ...
Abstract Background Wolfram syndrome (WS), caused by mutations of the Wolfram syndrome 1 (WFS1) gene...
Wolfram syndrome (WS) is a rare autosomal recessive disorder characterized by diabetes insipidus (DI...
Wolfram syndrome type 1 is a rare neurodegenerative disorder including diabetes insipidus, diabetes ...
PRESENTATION OF THE CASE Wolfram syndrome, named after the physician D J Wolfram is a rare inherit...
Wolfram syndrome is a rare autosomal recessive disorder characterized by optic atrophy and diabetes ...
Wolfram syndrome 1, a rare autosomal recessive neurodegenerative disease, is caused by mutations in ...
BACKGROUND: Wolfram Syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized...
Wolfram syndrome is a rare autosomal recessive disorder characterized by optic atrophy and diabetes ...
Item does not contain fulltextWolfram syndrome patients are mainly characterised by juvenile onset d...
Item does not contain fulltextWFS1 is a novel gene and encodes an 890 amino-acid glycoprotein (wolfr...
Wolfram (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness) syndrome is a rare auto...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed...
WFS1 is a novel gene and encodes an 890 amino-acid glycoprotein (wolframin), predominantly localized...
Item does not contain fulltextWolfram (diabetes insipidus, diabetes mellitus, optic atrophy, and dea...
OBJECTIVE\u2014 Wolfram syndrome is an autosomal recessive neurodegenerative disorder characterized ...
Abstract Background Wolfram syndrome (WS), caused by mutations of the Wolfram syndrome 1 (WFS1) gene...
Wolfram syndrome (WS) is a rare autosomal recessive disorder characterized by diabetes insipidus (DI...
Wolfram syndrome type 1 is a rare neurodegenerative disorder including diabetes insipidus, diabetes ...
PRESENTATION OF THE CASE Wolfram syndrome, named after the physician D J Wolfram is a rare inherit...
Wolfram syndrome is a rare autosomal recessive disorder characterized by optic atrophy and diabetes ...
Wolfram syndrome 1, a rare autosomal recessive neurodegenerative disease, is caused by mutations in ...
BACKGROUND: Wolfram Syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized...
Wolfram syndrome is a rare autosomal recessive disorder characterized by optic atrophy and diabetes ...