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A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family.
Khan, Anwar Kamal; Muhammad, Noor; Aziz, Abdul; Khan, Sher Alam; Shah, Khadim; Nasir, Abdul; Khan, Muzammil Ahmad; Khan, Saadullah.
Afiliação
  • Khan AK; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, 26000, Khyber Pakhtunkhwa, Pakistan.
  • Muhammad N; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, 26000, Khyber Pakhtunkhwa, Pakistan.
  • Aziz A; Department of Bioinformatics, Khushal Khan Khattak University, Karak, Pakistan.
  • Khan SA; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, 26000, Khyber Pakhtunkhwa, Pakistan.
  • Shah K; Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
  • Nasir A; Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
  • Khan MA; Gomal Centre of Biochemistry & Biotechnology, Gomal University, D.I.Khan, Pakistan.
  • Khan S; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, 26000, Khyber Pakhtunkhwa, Pakistan. saadkhanwazir@gmail.com.
BMC Med Genet ; 18(1): 42, 2017 04 12.
Article em En | MEDLINE | ID: mdl-28403827
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Displasia Ectodérmica / Proteínas de Homeodomínio Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: BMC Med Genet Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Displasia Ectodérmica / Proteínas de Homeodomínio Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: BMC Med Genet Ano de publicação: 2017 Tipo de documento: Article