[HTML][HTML] A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and …

A Pera, M Villamar, A Vinuela, M Gandía… - European Journal of …, 2008 - nature.com
Pendred syndrome (PS) and DFNB4, a non-syndromic sensorineural hearing loss with
enlargement of the vestibular aqueduct (EVA), are caused by mutations in the SLC26A4 …

[引用][C] A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and …

A PERA, M VILLAMAR, A VINUELA… - European journal of …, 2008 - pascal-francis.inist.fr
A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides
new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss CNRS …

[引用][C] A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and …

A Pera, M Villamar, A Viñuela, M Gandía… - European Journal of …, 2008 - cir.nii.ac.jp
A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides
new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss. | CiNii …

[PDF][PDF] A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and …

A Pera, M Villamar, A Vinuela, M Gandıa… - European Journal of …, 2008 - academia.edu
Introduction Mutations in the SLC26A4 gene cause Pendred's syndrome 1 (PS; MIM#
274600) and DFNB4, 2 the latter being a nonsyndromic form of hearing loss (MIM# 600791) …

A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 …

A Pera, M Villamar, A Viñuela… - … journal of human …, 2008 - pubmed.ncbi.nlm.nih.gov
Pendred syndrome (PS) and DFNB4, a non-syndromic sensorineural hearing loss with
enlargement of the vestibular aqueduct (EVA), are caused by mutations in the SLC26A4 …

A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 …

A Pera, M Villamar, A Viñuela, M Gandía… - European Journal of …, 2008 - europepmc.org
Pendred syndrome (PS) and DFNB4, a non-syndromic sensorineural hearing loss with
enlargement of the vestibular aqueduct (EVA), are caused by mutations in the SLC26A4 …

[PDF][PDF] A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and …

A Pera, M Villamar, A Vinuela, M Gandıa… - European Journal of …, 2008 - researchgate.net
Introduction Mutations in the SLC26A4 gene cause Pendred's syndrome 1 (PS; MIM#
274600) and DFNB4, 2 the latter being a nonsyndromic form of hearing loss (MIM# 600791) …

A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 …

A Pera, M Villamar, A Viñuela… - … Journal of Human …, 2008 - search.ebscohost.com
Pendred syndrome (PS) and DFNB4, a non-syndromic sensorineural hearing loss with
enlargement of the vestibular aqueduct (EVA), are caused by mutations in the SLC26A4 …

A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 …

A Pera, M Villamar, A Viñuela… - … Journal of Human …, 2008 - search.ebscohost.com
Pendred syndrome (PS) and DFNB4, a non-syndromic sensorineural hearing loss with
enlargement of the vestibular aqueduct (EVA), are caused by mutations in the SLC26A4 …

[引用][C] A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and …

A Pera, M Villamar, A Viñuela… - … Journal of Human …, 2008 - Nature Publishing Group