<p>*M, male; F, female; DM, diabetes mellitus; OA, optic atrophy; D, deafness; DI, diabetes insipidus, numbers indicate age at onset in years; +, symptomatic with unknown onset age; −, asymptomatic, Y; Yes, N; No, N/A; not applicable, □; consanguineous marriage and affected siblings.</p>§<p>Individual with detectable <i>WFS1</i> mutation in single chromosome.</p><p>Clinical characteristics and family history of each patient screened for <i>WFS1</i> mutations.</p
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 ...
OBJECTIVE — Wolfram syndrome is an extremely rare autosomal-recessive disorder that predisposes the ...
<p>Clinical features of affected family members associated with <i>WFS1</i> mutations found in this ...
<p>Ages at onset of both diabetes mellitus (A) and optic atrophy (B) in each patient in the three gr...
<p>Arrows show the probands in each family. Genetic findings for each individual tested are noted in...
Purpose: Wolfram syndrome is a degenerative, recessive rare disease with an onset in childhood. It i...
<div><p>Background</p><p>Wolfram syndrome (WFS) is a recessive neurologic and endocrinologic degener...
mutations to clinical manifestations in Japanese patients with WFS. was performed by direct sequenc...
International audiencePURPOSE:To search for WFS1 mutations in patients with optic atrophy (OA) and a...
OBJECTIVE\u2014 Wolfram syndrome is an autosomal recessive neurodegenerative disorder characterized ...
Wolfram Syndrome (WS) is a rare hereditary disease with autosomal recessive inheritance with incompl...
Item does not contain fulltextWolfram (diabetes insipidus, diabetes mellitus, optic atrophy, and dea...
Aims/hypothesis Wolfram syndrome is a rare, autosomal recessive syndrome characterised by juvenile-o...
Wolfram syndrome is a rare autosomal recessive disorder characterized by optic atrophy and diabetes ...
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 ...
OBJECTIVE — Wolfram syndrome is an extremely rare autosomal-recessive disorder that predisposes the ...
<p>Clinical features of affected family members associated with <i>WFS1</i> mutations found in this ...
<p>Ages at onset of both diabetes mellitus (A) and optic atrophy (B) in each patient in the three gr...
<p>Arrows show the probands in each family. Genetic findings for each individual tested are noted in...
Purpose: Wolfram syndrome is a degenerative, recessive rare disease with an onset in childhood. It i...
<div><p>Background</p><p>Wolfram syndrome (WFS) is a recessive neurologic and endocrinologic degener...
mutations to clinical manifestations in Japanese patients with WFS. was performed by direct sequenc...
International audiencePURPOSE:To search for WFS1 mutations in patients with optic atrophy (OA) and a...
OBJECTIVE\u2014 Wolfram syndrome is an autosomal recessive neurodegenerative disorder characterized ...
Wolfram Syndrome (WS) is a rare hereditary disease with autosomal recessive inheritance with incompl...
Item does not contain fulltextWolfram (diabetes insipidus, diabetes mellitus, optic atrophy, and dea...
Aims/hypothesis Wolfram syndrome is a rare, autosomal recessive syndrome characterised by juvenile-o...
Wolfram syndrome is a rare autosomal recessive disorder characterized by optic atrophy and diabetes ...
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 ...
OBJECTIVE — Wolfram syndrome is an extremely rare autosomal-recessive disorder that predisposes the ...