Biallelic mutations in pakistani families with autosomal recessive prelingual nonsyndromic hearing loss.

Choi, Hee Ji; Kanwal, Sumaira; Hameed, Rashid; Tamanna, Nasrin; Perveen, Shazia; Mahreen, Hina; Son, Wonseok; Lee, Kyung Suk; Chung, Ki Wha

Choi, Hee Ji; Kanwal, Sumaira; Hameed, Rashid; Tamanna, Nasrin; Perveen, Shazia; Mahreen, Hina; Son, Wonseok; Lee, Kyung Suk; Chung, Ki Wha.

Afiliação

Choi HJ; Department of Biological Sciences, Kongju National University, 56 Gongjudaehak-ro, Gongju, 32588, Korea.
Kanwal S; Department of Biosciences, COMSATS University Islamabad, Sahiwal, Pakistan.
Hameed R; DHQ Hospital Okara, Tehsil Road, Okara, Pakistan.
Tamanna N; Department of Biological Sciences, Kongju National University, 56 Gongjudaehak-ro, Gongju, 32588, Korea.
Perveen S; Department of Zoology, The Women University Multan, Multan, Punjab, Pakistan.
Mahreen H; Department of Zoology, The Women University Multan, Multan, Punjab, Pakistan.
Son W; Department of Biological Sciences, Kongju National University, 56 Gongjudaehak-ro, Gongju, 32588, Korea.
Lee KS; Department of Physics Education, Kongju National University, 56 Gongjudaehak-ro, Gongju, 32588, Korea.
Chung KW; Department of Biological Sciences, Kongju National University, 56 Gongjudaehak-ro, Gongju, 32588, Korea. kwchung@kongju.ac.kr.

Genes Genomics ; 45(2): 145-156, 2023 Feb.

Article em En | MEDLINE | ID: mdl-36472766

Assuntos

Surdez; Humanos; Paquistão; Surdez/genética; Mutação; Homozigoto; Proteínas Tirosina Fosfatases Classe 3 Semelhantes a Receptores/genética

Palavras-chave

Autosomal recessive hearing loss (DFNB); GJB2; LOXHD1; MYO15A; Pakistan; SLC26A4; TMC1

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Surdez Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Genes Genomics Ano de publicação: 2023 Tipo de documento: Article

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