TY  - GEN
AU  - Hogewind,Barend F T
AU  - Pennings,Ronald J E
AU  - Hol,Frans A
AU  - Kunst,Henricus P M
AU  - Hoefsloot,Elisabeth H
AU  - Cruysberg,Johannes R M
AU  - Cremers,Cor W R J
TI  - Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1
SN  - 1090-0535
PY  - 2010///0310
KW  - Adult
KW  - Aged, 80 and over
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Conserved Sequence
KW  - DNA Mutational Analysis
KW  - Diabetes Mellitus
KW  - genetics
KW  - Evolution, Molecular
KW  - Family
KW  - Female
KW  - Genes, Dominant
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Hearing Loss, Sensorineural
KW  - complications
KW  - Hearing Tests
KW  - Humans
KW  - Male
KW  - Membrane Proteins
KW  - chemistry
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Ocular Physiological Phenomena
KW  - Optic Nerve Diseases
KW  - Pedigree
KW  - Phenotype
KW  - Young Adult
N1  - Publication Type: Journal Article
ER  -