Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss

K Honda, AJ Griffith - Human genetics, 2022 - Springer
Mutations of coding regions and splice sites of SLC26A4 cause Pendred syndrome and
nonsyndromic recessive hearing loss DFNB4. SLC26A4 encodes pendrin, a …
被引用次数：46 相关文章

Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss.

K Honda, AJ Griffith - Human Genetics, 2022 - search.ebscohost.com
Mutations of coding regions and splice sites of SLC26A4 cause Pendred syndrome and
nonsyndromic recessive hearing loss DFNB4. SLC26A4 encodes pendrin, a …

[引用][C] Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss

K Honda, AJ Griffith - Human Genetics, 2021 - cir.nii.ac.jp
Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss | CiNii
Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 …

Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss

H Keiji, AJ Griffith - Human Genetics, 2022 - search.proquest.com
Mutations of coding regions and splice sites of SLC26A4 cause Pendred syndrome and
nonsyndromic recessive hearing loss DFNB4. SLC26A4 encodes pendrin, a …

Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss

K Honda, AJ Griffith - Human genetics, 2022 - pubmed.ncbi.nlm.nih.gov
Mutations of coding regions and splice sites of SLC26A4 cause Pendred syndrome and
nonsyndromic recessive hearing loss DFNB4. SLC26A4 encodes pendrin, a …

Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss.

K Honda, AJ Griffith - Human Genetics, 2021 - europepmc.org
Mutations of coding regions and splice sites of SLC26A4 cause Pendred syndrome and
nonsyndromic recessive hearing loss DFNB4. SLC26A4 encodes pendrin, a …