A new case of Kaufman Oculocerebrofacial Syndrome caused by two new splicing variants in UBE3B. - Université de Rennes Accéder directement au contenu
Article Dans Une Revue European Journal of Human Genetics Année : 2020

A new case of Kaufman Oculocerebrofacial Syndrome caused by two new splicing variants in UBE3B.

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Dates et versions

hal-03131644 , version 1 (04-02-2021)

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  • HAL Id : hal-03131644 , version 1

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K. Uguen, C. Ka, M. Planes, S. Audebert-Bellanger, S. Redon, et al.. A new case of Kaufman Oculocerebrofacial Syndrome caused by two new splicing variants in UBE3B.. European Journal of Human Genetics, 2020, 28 (SUPPL 1), pp.366-367. ⟨hal-03131644⟩
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