Your browser doesn't support javascript.
loading
Molecular insight into CREBBP and TANGO2 variants causing intellectual disability.
Hussain, Syeda Iqra; Muhammad, Nazif; Khan, Niamatullah; Khan, Mobeen; Fardous, Fardous; Tahir, Raheel; Yasin, Muhammad; Khan, Sher Alam; Saleha, Shamim; Muhammad, Noor; Wasif, Naveed; Khan, Saadullah.
Afiliação
  • Hussain SI; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Muhammad N; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Khan N; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Khan M; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Fardous F; Department of Medical Lab Technology, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Tahir R; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Yasin M; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Khan SA; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Saleha S; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Muhammad N; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.
  • Wasif N; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.
  • Khan S; Institute of Human Genetics, University Hospital Schleswig-Holstein, Kiel, Germany.
J Gene Med ; 26(1): e3591, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37721116
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rabdomiólise / Síndrome de Rubinstein-Taybi / Deficiência Intelectual Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: J Gene Med Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Paquistão
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rabdomiólise / Síndrome de Rubinstein-Taybi / Deficiência Intelectual Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: J Gene Med Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Paquistão