Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA
A Pera, S Dossena, S Rodighiero, M Gandía… - … OF THE NATIONAL …, 2008 - air.unimi.it
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA
A Pera, S Dossena, S Rodighiero… - Proceedings of the …, 2008 - pubmed.ncbi.nlm.nih.gov
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA
A Pera, S Dossena, S Rodighiero, M Gandía… - Proceedings of the …, 2008 - cir.nii.ac.jp
抄録< jats: p> Pendred syndrome is an autosomal recessive disorder characterized by
sensorineural hearing loss, with malformations of the inner ear, ranging from enlarged …
sensorineural hearing loss, with malformations of the inner ear, ranging from enlarged …
Functional Assessment of Allelic Variants in the SLC26A4 Gene Involved in Pendred Syndrome and Nonsyndromic EVA
A Pera, S Dossena, S Rodighiero, M Gandía… - Proceedings of the …, 2008 - JSTOR
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
[HTML][HTML] Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA
A Pera, S Dossena, S Rodighiero… - Proceedings of the …, 2008 - ncbi.nlm.nih.gov
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA.
A Pera, S Dossena, S Rodighiero… - Proceedings of the …, 2008 - europepmc.org
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
[PDF][PDF] Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA
A Peraa, S Dossenab, S Rodighieroc, M Gandíaa… - PNAS, 2008 - researchgate.net
Results Mutations of the SLC26A4 Gene Found in the Normal-Hearing Spanish Population.
In our cohort of 214 normal-hearing Spanish subjects, we identified a total of 17 allelic …
In our cohort of 214 normal-hearing Spanish subjects, we identified a total of 17 allelic …
[PDF][PDF] Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA
A Peraa, S Dossenab, S Rodighieroc, M Gandíaa… - PNAS, 2008 - academia.edu
Results Mutations of the SLC26A4 Gene Found in the Normal-Hearing Spanish Population.
In our cohort of 214 normal-hearing Spanish subjects, we identified a total of 17 allelic …
In our cohort of 214 normal-hearing Spanish subjects, we identified a total of 17 allelic …
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA
A Pera, S Dossena, S Rodighiero… - Proceedings of the …, 2008 - ui.adsabs.harvard.edu
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …
hearing loss, with malformations of the inner ear, ranging from enlarged vestibular aqueduct …