Noggin heterozygous mice: an animal model for congenital conductive hearing loss in humans (original) (raw)

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A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness ( dn ) locus

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Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

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Mapping and Characterization of a Novel Cochlear Gene in Human and in Mouse: A Positional Candidate Gene for a Deafness Disorder, DFNA9

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Molecular Etiology of Deafness and Cochlear Consequences

Zippora Brownstein

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Noncoding microdeletion in mouseHgfdisrupts neural crest migration into the stria vascularis, reduces the endocochlear potential and suggests the neuropathology for human nonsyndromic deafness DFNB39

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A new mouse insertional mutation that causes sensorineural deafness and vestibular defects

Lisa Stubbs

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Cochlear homeostasis and its role in genetic deafness

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A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells

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Molecular genetics of nonsyndromic deafness

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A Point Mutation in the Gene for Asparagine-Linked Glycosylation 10B (Alg10b) Causes Nonsyndromic Hearing Impairment in Mice (Mus musculus)

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At the Speed of Sound: Gene Discovery in the Auditory System

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MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

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Measurement of conductive hearing loss in mice

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Unique Transgenic Animal Model for Hereditary Hearing Loss

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Mutation of the POU-domain gene Brn4/Pou3f4 affects middle-ear sound conduction in the mouse

E Bryan Crenshaw III

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