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Exome sequencing identifies homozygous variants in MBOAT7 associated with neurodevelopmental disorder.
Nazmina, Gul; Khan, Amjad; Jiang, Jiuhong; Miao, Zhichao; Khan, Shahid Niaz; Khan, Muhammad Ismail; Shah, Abdul Haleem; Shah, Ayesha Haleem; Khisroon, Muhammad; Haack, Tobias B.
Afiliação
  • Nazmina G; Department of Zoology, University of Peshawar, Peshawar, Pakistan.
  • Khan A; Faculty of Biological Sciences, Department of Zoology, University of Lakki Marwat, Khyber Pakhtunkhwa, Pakistan.
  • Jiang J; Institute for Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Miao Z; Alexander von Humboldt Fellowship Foundation, Berlin, Germany.
  • Khan SN; Guangzhou National Laboratory, Guangzhou International Bio Island, Guangzhou, China.
  • Khan MI; GMU-GIBH Joint School of Life Sciences, The Guangdong-Hong Kong-Macau Joint Laboratory for Cell Fate Regulation and Diseases, Guangzhou National Laboratory, Guangzhou Medical University, Guangzhou, China.
  • Shah AH; Shanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Clinical Research Center for Anesthesiology and Perioperative Medicine Translational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People's Hospital, School of Medicine, Tongji University, Shanghai,
  • Shah AH; Department of Zoology, Kohat University of Science and Technology, Kohat, Pakistan.
  • Khisroon M; Department of Zoology, Islamia College University Peshawar, Peshawar, Pakistan.
  • Haack TB; Institute of Biological sciences, Gomal University, Dera Ismail Khan, Pakistan.
Clin Genet ; 105(4): 423-429, 2024 04.
Article em En | MEDLINE | ID: mdl-38088234
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Deficiência Intelectual / Malformações do Sistema Nervoso Limite: Humans / Newborn Idioma: En Revista: Clin Genet Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Paquistão
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Deficiência Intelectual / Malformações do Sistema Nervoso Limite: Humans / Newborn Idioma: En Revista: Clin Genet Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Paquistão