The implication of holocytochrome c synthase mutation in Korean familial hypoplastic amelogenesis imperfecta.

Choi, Hyejin; Lee, Kwanghwan; Kim, Donghyo; Kim, Sanguk; Lee, Jae Hoon

Choi, Hyejin; Lee, Kwanghwan; Kim, Donghyo; Kim, Sanguk; Lee, Jae Hoon.

Afiliação

Choi H; Department of Prosthodontics, College of Dentistry at Yonsei University, 50-1 Yonsei-ro, Seodaemoon-gu, Seoul, 120-752, Republic of Korea.
Lee K; Department of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Kim D; Department of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Kim S; Department of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea. sukim@postech.ac.kr.
Lee JH; Department of Prosthodontics, College of Dentistry at Yonsei University, 50-1 Yonsei-ro, Seodaemoon-gu, Seoul, 120-752, Republic of Korea. jaehoon115@yuhs.ac.

Clin Oral Investig ; 26(6): 4487-4498, 2022 Jun.

Article em En | MEDLINE | ID: mdl-35243551

Assuntos

Amelogênese Imperfeita; Amelogênese Imperfeita/genética; Odontólogos; Humanos; Liases; Mutação; Papel Profissional; República da Coreia

Palavras-chave

Amelogenesis imperfecta; Bioinformatics analysis; HCCS; Korean population; Whole-exome sequencing

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amelogênese Imperfeita Tipo de estudo: Prognostic_studies / Screening_studies Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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