De novo nonsense mutation in WHSC1 (NSD2) in patient with...

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Journal of Human Genetics 2018 / 5

De novo nonsense mutation in WHSC1 (NSD2) in patient with intellectual disability and dysmorphic features

Lozier, Ekaterina R., Konovalov, Fedor A., Kanivets, Ilya V., Pyankov, Denis V., Koshkin, Philip A., Baleva, Larisa S., Sipyagina, Alla E., Yakusheva, Elena N., Kuchina, Anastasiya E., Korostelev, Ser
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Language:
english
Journal:
Journal of Human Genetics
DOI:
10.1038/s10038-018-0464-5
Date:
May, 2018
File:
PDF, 512 KB
english, 2018
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