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Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree

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Description scientific article published on 16 July 2016
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author: Periklis Makrythanasis  Muhammad Ansar  Michel Guipponi  Federico A Santoni  Stilianos Antonarakis  Maha Zaki  Mahmoud Y Issa 

Publication date July 16, 2016
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