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1
Genetic Hearing Loss
CRC Press
Patrick J. Willems
hearing
mutations
gene
syndrome
deafness
mutation
genet
genes
mouse
protein
myosin
impairment
autosomal
hum
vestibular
function
cochlea
identified
nonsyndromic
different
mice
patients
cochlear
factors
analysis
diaphanous
mitochondrial
clinical
auditory
proteins
affected
phenotype
chromosome
usher
individuals
recessive
sensorineural
molecular
missense
exon
transcription
cases
membrane
expressed
studies
amino
first
biol
hcs
coch
年:
2003
语言:
english
文件:
PDF, 7.06 MB
您的标签:
0
/
0
english, 2003
2
Genetic hearing loss
Marcel Dekker
Patrick J. Willems
hearing
mutations
gene
syndrome
deafness
mutation
genet
genes
mouse
protein
myosin
impairment
autosomal
hum
vestibular
function
cochlea
identified
nonsyndromic
different
mice
patients
cochlear
factors
analysis
diaphanous
mitochondrial
clinical
auditory
proteins
affected
phenotype
chromosome
usher
individuals
recessive
sensorineural
molecular
missense
exon
transcription
cases
membrane
expressed
studies
amino
first
biol
hcs
coch
年:
2004
语言:
english
文件:
PDF, 5.60 MB
您的标签:
0
/
4.0
english, 2004
3
Genetic Hearing Loss
Marcel Dekker
Patrick J. Willems
hearing
mutations
gene
syndrome
deafness
mutation
genet
genes
mouse
protein
myosin
impairment
autosomal
hum
vestibular
function
cochlea
identified
nonsyndromic
different
mice
patients
cochlear
factors
analysis
diaphanous
mitochondrial
clinical
auditory
proteins
affected
phenotype
chromosome
usher
individuals
recessive
sensorineural
molecular
missense
exon
transcription
cases
membrane
expressed
studies
amino
first
biol
hcs
coch
年:
2004
语言:
english
文件:
PDF, 7.06 MB
您的标签:
0
/
0
english, 2004
4
Mechanotransduction of the Hair Cell
Springer Singapore
Wei Xiong
,
Zhigang Xu
stereocilia
pcdh15
journal
channels
mice
gene
tmc1
cochlear
protein
mechanotransduction
molecular
auditory
cdh23
hearing
proteins
mouse
adaptation
tmc2
membrane
cib2
harmonin
neuroscience
genetics
tmie
bundle
transduction
complex
lhfpl5
calcium
transmembrane
components
function
mutations
cochlea
current
machinery
deafness
usher
cadherin
showed
syndrome
polarity
xiong
component
mammalian
knockout
localization
sensory
expressed
mutation
年:
2018
语言:
english
文件:
PDF, 1.67 MB
您的标签:
0
/
0
english, 2018
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