[HTML][HTML] Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

M Li, S Nishio, C Naruse, M Riddell, S Sapski… - Nature …, 2020 - nature.com
Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …

[引用][C] Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

M Li, S Nishio, C Naruse, M Riddell, S Sapski… - NATURE …, 2020 - pure.mpg.de

Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

西尾, 信哉, 成瀬, 智恵, 勝野, 匹田, 貴夫… - Nature …, 2020 - cir.nii.ac.jp
抄録 Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …

Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

M Li, S Nishio, C Naruse, M Riddell… - Nature …, 2020 - repository.kulib.kyoto-u.ac.jp
Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …

Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome.

M Li, S Nishio, C Naruse, M Riddell… - Nature …, 2020 - search.ebscohost.com
Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …

[HTML][HTML] Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

M Li, S Nishio, C Naruse, M Riddell… - Nature …, 2020 - ncbi.nlm.nih.gov
Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …

Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome.

M Li, SY Nishio, C Naruse, M Riddell… - Nature …, 2020 - europepmc.org
Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …

Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

M Li, S Nishio, C Naruse, M Riddell, S Sapski… - Nature …, 2020 - ideas.repec.org
Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …

Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

M Li, SY Nishio, C Naruse, M Riddell… - Nature …, 2020 - pubmed.ncbi.nlm.nih.gov
Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …

[PDF][PDF] Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

M Li, S Nishio, C Naruse, M Riddell… - Nature …, 2020 - scholar.archive.org
Enlarged vestibular aqueduct (EVA) is one of the most commonly identified inner ear
malformations in hearing loss patients including Pendred syndrome. While biallelic …