Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

T Kojima, K Wasano, S Takahashi… - Disease Models & …, 2021 - journals.biologists.com
ABSTRACT KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel
Kv7. 4, and is the causative gene for autosomal dominant nonsyndromic sensorineural …
被引用次数：8 相关文章

Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

T Kojima, K Wasano… - … Disease Models and …, 2021 - scholars.northwestern.edu
KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel Kv7. 4, and
is the causative gene for autosomal dominant nonsyndromic sensorineural hearing loss …

Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

T Kojima, K Wasano, S Takahashi… - Disease Models & …, 2021 - cir.nii.ac.jp
抄録< jats: title> ABSTRACT</jats: title>< jats: p> KCNQ4 encodes the homotetrameric
voltage-dependent potassium ion channel Kv7. 4, and is the causative gene for autosomal …
[PDF] semanticscholar.org

[PDF][PDF] Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

T Kojima, K Wasano, S Takahashi, K Homma - 2021 - pdfs.semanticscholar.org
In vitro evidence for normal hearing of V499G/Y501H prestin heterozygous mice (499 het)
Page 1 © 2021. Published by The Company of Biologists Ltd. This is an Open Access article …

Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

T Kojima, K Wasano, S Takahashi… - Disease Models & …, 2021 - search.proquest.com
KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel Kv7. 4, and
is the causative gene for autosomal dominant nonsyndromic sensorineural hearing loss …

Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

T Kojima, K Wasano, S Takahashi… - Disease models & …, 2021 - pubmed.ncbi.nlm.nih.gov
KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel Kv7. 4, and
is the causative gene for autosomal dominant nonsyndromic sensorineural hearing loss …
[HTML] nih.gov

[HTML][HTML] Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

T Kojima, K Wasano, S Takahashi… - Disease Models & …, 2021 - ncbi.nlm.nih.gov
ABSTRACT KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel
Kv7. 4, and is the causative gene for autosomal dominant nonsyndromic sensorineural …
[PDF] biologists.com

[PDF][PDF] Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

T Kojima, K Wasano, S Takahashi… - Disease Models & …, 2021 - journals.biologists.com
ABSTRACT KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel
Kv7. 4, and is the causative gene for autosomal dominant nonsyndromic sensorineural …

Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss.

T Kojima, K Wasano, S Takahashi… - Disease Models & …, 2021 - europepmc.org
ABSTRACT KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel
Kv7. 4, and is the causative gene for autosomal dominant nonsyndromic sensorineural …

Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss.

T Kojima, K Wasano, S Takahashi… - Disease Models & …, 2021 - europepmc.org
ABSTRACT KCNQ4 encodes the homotetrameric voltage-dependent potassium ion channel
Kv7. 4, and is the causative gene for autosomal dominant nonsyndromic sensorineural …