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[HTML][HTML] Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E Lopez-Martin, A Martinez-Monseny… - Orphanet Journal of …, 2020 - Springer
Background Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are
associated with a newly identified neurodevelopmental disorder characterized mainly by …
被引用次数：27 相关文章

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum.

R Urreizti, E Lopez-Martin… - Orphanet Journal of …, 2020 - europepmc.org
Background Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are
associated with a newly identified neurodevelopmental disorder characterized mainly by …

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E López-Martin… - Orphanet Journal of …, 2020 - diposit.ub.edu
Background: Pathogenic variants of the lysine acetyltransferase 6A orKAT6Agene are
associated with a newlyidentified neurodevelopmental disorder characterized mainly by …

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E Lopez-Martin… - Orphanet Journal of …, 2020 - go.gale.com
Background Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are
associated with a newly identified neurodevelopmental disorder characterized mainly by …

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E Lopez-Martin, A Martinez-Monseny… - 2020 - search.proquest.com
Background Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are
associated with a newly identified neurodevelopmental disorder characterized mainly by …
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[HTML][HTML] Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E Lopez-Martin… - … Journal of Rare …, 2020 - ojrd.biomedcentral.com
Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are associated with a
newly identified neurodevelopmental disorder characterized mainly by intellectual disability …

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E Lopez-Martin… - Orphanet journal of …, 2020 - pubmed.ncbi.nlm.nih.gov
Background Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are
associated with a newly identified neurodevelopmental disorder characterized mainly by …

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E Lopez-Martin… - Orphanet Journal of …, 2020 - jglobal.jst.go.jp
Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the
molecular and clinical spectrum | Article Information | J-GLOBAL Art J-GLOBAL ID:202002264066474371 …

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E Lopez-Martin… - … Journal of Rare …, 2020 - research.sahmri.org.au
Background: Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are
associated with a newly identified neurodevelopmental disorder characterized mainly by …
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[HTML][HTML] Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

R Urreizti, E Lopez-Martin… - Orphanet Journal of …, 2020 - ncbi.nlm.nih.gov
Background Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are
associated with a newly identified neurodevelopmental disorder characterized mainly by …