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UnknownWhole-exome sequencing and its impact in hereditary hearing loss.
Not available
S-EPMC5503681 | biostudies-literature
UnknownRipor2 is involved in auditory hair cell stereociliary bundle structure and orientation.
Not available
S-EPMC6238639 | biostudies-literature
UnknownPedometers to enhance physical activity in COPD: a randomised controlled trial.
Not available
S-EPMC4318658 | biostudies-literature
UnknownWhole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.
Not available
S-EPMC3511533 | biostudies-literature
UnknownDysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss.
Not available
S-EPMC6347722 | biostudies-literature
UnknownMPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.
Not available
S-EPMC6478175 | biostudies-literature
UnknownFAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.
Not available
S-EPMC4103326 | biostudies-literature
UnknownSLITRK6 mutations cause myopia and deafness in humans and mice.
Not available
S-EPMC3635725 | biostudies-literature
UnknownROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.
Not available
S-EPMC4889368 | biostudies-literature
UnknownFOXF2 is required for cochlear development in humans and mice.
Not available
S-EPMC6452198 | biostudies-literature
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