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Whole exome sequencing identifies a novel variant causing cockayne syndrome type I in a consanguineous Pakistani family.
Zulfiqar, Shumaila; Moawia, Abubakar; Waseem, Syeda Seema; Ali, Zafar; Ramzan, Shafaq; Anjum, Iram; Baig, Shahid Mahmood; Tariq, Muhammad.
Afiliação
  • Zulfiqar S; Department of Biotechnology, Kinnaird College for Women, Lahore, Pakistan.
  • Moawia A; Institute of Human Genetics, Ulm University and Ulm University Medical Centre, Ulm, Germany.
  • Waseem SS; Cologne Center for Genomics (CCG), Faculty of Medicine, University Hospital, University of Cologne, Cologne, Germany.
  • Ali Z; Centre for Biotechnology and Microbiology, University of Swat, Swat, Pakistan.
  • Ramzan S; National Institute for Biotechnology and Genetic Engineering College (NIBGE-C), Faisalabad, Pakistan Institute of Engineering and Applied Sciences (PIEAS), Islamabad, Pakistan.
  • Anjum I; Department of Biotechnology, Kinnaird College for Women, Lahore, Pakistan.
  • Baig SM; National Institute for Biotechnology and Genetic Engineering College (NIBGE-C), Faisalabad, Pakistan Institute of Engineering and Applied Sciences (PIEAS), Islamabad, Pakistan.
  • Tariq M; Pakistan Science Foundation, Islamabad, Pakistan.
Int J Neurosci ; : 1-6, 2022 Jun 12.
Article em En | MEDLINE | ID: mdl-35645363
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article