A novel in-frame deletion of OPHN1 in a family with...

European Journal of Paediatric Neurology 2017 / 06 Vol. 21

A novel in-frame deletion of OPHN1 in a family with syndromic X-linked mental retardation

Brankovic, V., Nuovo, S., Zekavica, A., Micalizzi, A., Poretti, A., Valente, E.M.
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Volume:
21
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/j.ejpn.2017.04.900
Date:
June, 2017
File:
PDF, 41 KB
english, 2017
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