Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain

C Bassot, G Minervini, E Leonardi, SCE Tosatto - Biochimie, 2017 - Elsevier
Abstract Human pendrin (SLC26A4) is an anion transporter mostly expressed in the inner
ear, thyroid and kidney. SLC26A4 gene mutations are associated with a broad phenotypic …
被引用次数：23 相关文章

[引用][C] Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain

C Bassot, G Minervini, E Leonardi, S Tosatto - BIOCHIMIE, 2017 - research.unipd.it
Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4)
transmembrane domain IRIS IRIS Home Sfoglia Macrotipologie & tipologie Autore Titolo …

[引用][C] Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain

C Bassot, G Minervini, E Leonardi, SCE Tosatto - Biochimie, 2017 - cir.nii.ac.jp
Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4)
transmembrane domain | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] …

Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain

C Bassot, G Minervini, E Leonardi… - Biochimie, 2017 - pubmed.ncbi.nlm.nih.gov
Human pendrin (SLC26A4) is an anion transporter mostly expressed in the inner ear, thyroid
and kidney. SLC26A4 gene mutations are associated with a broad phenotypic spectrum …

Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain.

C Bassot, G Minervini, E Leonardi, SC Tosatto - Biochimie, 2016 - europepmc.org
Human pendrin (SLC26A4) is an anion transporter mostly expressed in the inner ear, thyroid
and kidney. SLC26A4 gene mutations are associated with a broad phenotypic spectrum …

Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain

C Bassot, G Minervini, E Leonardi, SCE Tosatto - Biochimie, 2017 - infona.pl
Human pendrin (SLC26A4) is an anion transporter mostly expressed in the inner ear, thyroid
and kidney. SLC26A4 gene mutations are associated with a broad phenotypic spectrum …

[引用][C] Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain

C Bassot, G Minervini, E Leonardi, SCE Tosatto - 2017