Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome.

Journal of molecular endocrinology, 2009 - europepmc.org
Pendred syndrome (PS) is the most frequent form of genetically related syndromic hearing
loss, and is associated with mutations of pendrin, encoded by the SLC26A4 gene. This …
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Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome

S Dossena, S Rodighiero, V Vezzoli… - JOURNAL OF …, 2009 - air.unimi.it
Pendred syndrome (PS) is the most frequent form of genetically related syndromic hearing
loss, and is associated with mutations of pendrin, encoded by the SLC26A4 gene. This …

[引用][C] Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome.

S Dossena, S Rodighiero, V Vezzoli… - JOURNAL OF …, 2009 - pure.pmu.ac.at
Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter
involved in Pendred syndrome. — PMU Forschungsportal Zur Hauptnavigation wechseln Zur …

Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome

S Dossena, S Rodighiero, V Vezzoli… - Journal of …, 2009 - pubmed.ncbi.nlm.nih.gov
Pendred syndrome (PS) is the most frequent form of genetically related syndromic hearing
loss, and is associated with mutations of pendrin, encoded by the SLC26A4 gene. This …

Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome

S Dossena, S Rodighiero, V Vezzoli… - Journal of Molecular …, 2009 - cir.nii.ac.jp
抄録< jats: p> Pendred syndrome (PS) is the most frequent form of genetically related
syndromic hearing loss, and is associated with mutations of pendrin, encoded by the< jats …

[引用][C] Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome.

S Dossena, S Rodighiero, V Vezzoli… - JOURNAL OF …, 2009 - pure.pmu.ac.at
Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter
involved in Pendred syndrome. — PMU Research Portal Skip to main navigation Skip to …

[引用][C] Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome

S DOSSENA - J. Mol. Endocrinol., 2009 - cir.nii.ac.jp
Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter
involved in Pendred syndrome | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ …

[引用][C] Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome

S DOSSENA, S RODIGHIERO, V VEZZOLI… - Journal of molecular …, 2009 - BioScientifica