Marilena Elpidorou
2PUBLICATIONS
2CO-AUTHORS

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Publications (2)
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|Feb 26, 2022
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease.Marilena Elpidorou, James A Poulter, Katarzyna Szymanska
|Jun 24, 2020
Novel loss-of-function mutation in HERC2 is associated with severe developmental delay and paediatric lethality.Marilena Elpidorou, Sunayna Best, James A Poulter
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