A novel mutation in SLC26A4 causes nonsyndromic autosomal recessive hearing impairment

A Wolf, A Frohne, M Allen, T Parzefall… - Otology & …, 2017 - journals.lww.com
Background: Heterozygous mutations in GJB2 (MIM: 121011) encoding the gap junction
protein connexin 26 are overrepresented in patient groups suffering from nonsyndromic …
被引用次数：11 相关文章

A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment.

A Wolf, A Frohne, M Allen, T Parzefall… - … : Official Publication of …, 2017 - europepmc.org
Background Heterozygous mutations in GJB2 (MIM: 121011) encoding the gap junction
protein connexin 26 are overrepresented in patient groups suffering from nonsyndromic …

A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment

A Wolf, A Frohne, M Allen… - … publication of the …, 2017 - pubmed.ncbi.nlm.nih.gov
Background Heterozygous mutations in GJB2 (MIM: 121011) encoding the gap junction
protein connexin 26 are overrepresented in patient groups suffering from nonsyndromic …