Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.

Moassass, Faten; Al-Halabi, Bassel; Nweder, Mohamad Sayah; Al-Achkar, Walid

Moassass, Faten; Al-Halabi, Bassel; Nweder, Mohamad Sayah; Al-Achkar, Walid.

Afiliação

Moassass F; Human Genetics Division, Molecular Biology and Biotechnology Department, Atomic Energy Commission, Damascus, Syria.
Al-Halabi B; Human Genetics Division, Molecular Biology and Biotechnology Department, Atomic Energy Commission, Damascus, Syria.
Nweder MS; Human Genetics Division, Molecular Biology and Biotechnology Department, Atomic Energy Commission, Damascus, Syria.
Al-Achkar W; Human Genetics Division, Molecular Biology and Biotechnology Department, Atomic Energy Commission, Damascus, Syria. Electronic address: ascientific14@aec.org.sy.

Int J Pediatr Otorhinolaryngol ; 113: 110-114, 2018 Oct.

Article em En | MEDLINE | ID: mdl-30173967

Assuntos

DNA Mitocondrial/genética; Perda Auditiva Neurossensorial/genética; Mutação; Adolescente; Criança; Pré-Escolar; Feminino; Genótipo; Humanos; Masculino; Síria

Palavras-chave

Mitochondria DNA; Mutations; Non- syndromic hearing loss (NSHL); Syrian

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Perda Auditiva Neurossensorial / Mutação Tipo de estudo: Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Int J Pediatr Otorhinolaryngol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Síria

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