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Issue Date
Title
Author(s)
2019
A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay
Mucha, B.E.
;
Banka, S.
;
Ajeawung, N.F.
;
Molidperee, S.
;
Chen, G.G.
;
Koenig, M.K.
;
Adejumo, R.B.
;
Till, M.
;
Harbord, M.
;
Perrier, R.
;
Lemyre, E.
;
Boucher, R.M.
;
Skotko, B.G.
;
Waxler, J.L.
;
Thomas, M.A.
;
Hodge, J.C.
;
Gecz, J.
;
Nicholl, J.
;
McGregor, L.
;
Linden, T.
;
et al.
Discover
Author
1
Adejumo, R.B.
1
Ajeawung, N.F.
1
Banka, S.
1
Boucher, R.M.
1
Chen, G.G.
1
et al.
1
Gecz, J.
1
Harbord, M.
1
Hodge, J.C.
1
Koenig, M.K.
.
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Subject
1
16p13.3
1
3-Phosphoinositide-Dependent Prot...
1
Adolescent
1
Adult
1
Child
1
Child, Preschool
1
Chromosome Deletion
1
Chromosomes, Human, Pair 16
1
Cohort Studies
1
Developmental Disabilities
.
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Date issued
1
2019