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Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree
scientific article published on 16 July 2016
Author/s
author: Periklis Makrythanasis, Federico A Santoni, Maha Zaki, Mahmoud Y Issa, Muhammad Ansar, Stylianos E. Antonarakis, Michel Guipponi
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Publication date
July 16, 2016
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