Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.

Abdel Megeid, Azza K; Refeat, Miral M; Ashaat, Engy A; El-Kamah, Ghada; El-Saiedi, Sonia A; Elfalaki, Mona M; El Ruby, Mona O; Amr, Khalda S

Abdel Megeid, Azza K; Refeat, Miral M; Ashaat, Engy A; El-Kamah, Ghada; El-Saiedi, Sonia A; Elfalaki, Mona M; El Ruby, Mona O; Amr, Khalda S.

Afiliação

Abdel Megeid AK; Pediatric Department, Cairo University, Giza, Egypt.
Refeat MM; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Ashaat EA; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
El-Kamah G; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
El-Saiedi SA; Pediatric Department, Cairo University, Giza, Egypt.
Elfalaki MM; Pediatric Department, Cairo University, Giza, Egypt.
El Ruby MO; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Amr KS; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt. khalda_nrc@yahoo.com.

J Genet Eng Biotechnol ; 20(1): 117, 2022 Aug 08.

Article em En | MEDLINE | ID: mdl-35939165

Palavras-chave

Childhood interstitial lung disease; ILD genetics; Surfactant protein C; Variants

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Genet Eng Biotechnol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito País de publicação: Holanda

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