TY  - GEN
AU  - Konigsmark,B W
TI  - Hereditary deafness in man
SN  - 0028-4793
PY  - 1969///1021
KW  - Abnormalities, Multiple
KW  - Adult
KW  - Ataxia
KW  - complications
KW  - Bone and Bones
KW  - abnormalities
KW  - Cataract
KW  - Child
KW  - Child, Preschool
KW  - Deafness
KW  - Diabetes Complications
KW  - Diabetes Mellitus, Type 1
KW  - Diabetic Neuropathies
KW  - Diabetic Retinopathy
KW  - Eye Diseases
KW  - Gait
KW  - Genes, Dominant
KW  - Genes, Recessive
KW  - Humans
KW  - Hypogonadism
KW  - Intellectual Disability
KW  - Kidney Diseases
KW  - Middle Aged
KW  - Muscular Diseases
KW  - Myoclonus
KW  - Myopia
KW  - Nervous System Diseases
KW  - Neurilemmoma
KW  - Nose Deformities, Acquired
KW  - Obesity
KW  - Optic Atrophy
KW  - Peripheral Nervous System Diseases
KW  - Refsum Disease
KW  - genetics
KW  - Retinitis Pigmentosa
KW  - Vestibulocochlear Nerve
N1  - Publication Type: Journal Article; Review
UR  - https://doi.org/10.1056/NEJM196910022811407
ER  -