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Ansar, Muhammad; Paracha, Sohail Aziz; Serretti, Alessandro; Sarwar, Muhammad T; Khan, Jamshed; Ranza, Emmanuelle; Falconnet, Emilie; Iwaszkiewicz, Justyna; Shah, Sayyed Fahim; Qaisar, Azhar Ali; Santoni, Federico A; Zoete, Vincent; Megarbane, Andre; Ahmed, Jawad; Colombo, Roberto; Makrythanasis, Periklis; Antonarakis, Stylianos E

Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature

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  • Media type: E-Article
  • Title: Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature
  • Contributor: Ansar, Muhammad; Paracha, Sohail Aziz; Serretti, Alessandro; Sarwar, Muhammad T; Khan, Jamshed; Ranza, Emmanuelle; Falconnet, Emilie; Iwaszkiewicz, Justyna; Shah, Sayyed Fahim; Qaisar, Azhar Ali; Santoni, Federico A; Zoete, Vincent; Megarbane, Andre; Ahmed, Jawad; Colombo, Roberto; Makrythanasis, Periklis; Antonarakis, Stylianos E
  • Published: Oxford University Press (OUP), 2019
  • Published in: Human Molecular Genetics, 28 (2019) 6, Seite 972-979
  • Language: English
  • DOI: 10.1093/hmg/ddy406
  • ISSN: 0964-6906; 1460-2083
  • Origination:
  • Footnote:
  • Access State: Open Access