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A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review.
Mir, Atefeh; Song, Yongjun; Lee, Hane; Montazer-Zohouri, Mostafa; Reisi, Marziyeh; Tabatabaiefar, Mohammad Amin.
Affiliation
  • Mir A; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Song Y; Division of Medical Genetics, 3Billion Inc, Seoul, South Korea.
  • Lee H; Division of Medical Genetics, 3Billion Inc, Seoul, South Korea.
  • Montazer-Zohouri M; Genetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.
  • Reisi M; Department of Immunology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
  • Tabatabaiefar MA; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Mol Genet Genomic Med ; 11(12): e2261, 2023 Dec.
Article in En | MEDLINE | ID: mdl-37496384
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intellectual Disability Type of study: Guideline / Prognostic_studies Limits: Child / Humans Language: En Journal: Mol Genet Genomic Med Year: 2023 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intellectual Disability Type of study: Guideline / Prognostic_studies Limits: Child / Humans Language: En Journal: Mol Genet Genomic Med Year: 2023 Document type: Article Affiliation country: