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National Institutes of Health
USHER SYNDROME, TYPE IB (disorder)
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Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
P. M. Kelley
American journal of human genetics
Corpus ID: 2340288
Usher syndrome type 1b (USH1B) is an autosomal recessive disorder characterized by congenital profound hearing loss, vestibular…
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