Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
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Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
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Whole exome sequencing identif ...... primary, autosomal recessive.
@en
Whole exome sequencing identif ...... primary, autosomal recessive.
@nl
type
label
Whole exome sequencing identif ...... primary, autosomal recessive.
@en
Whole exome sequencing identif ...... primary, autosomal recessive.
@nl
prefLabel
Whole exome sequencing identif ...... primary, autosomal recessive.
@en
Whole exome sequencing identif ...... primary, autosomal recessive.
@nl
P2093
P2860
P1433
P1476
Whole exome sequencing identif ...... , primary, autosomal recessive
@en
P2093
Desaraju Suresh Bhargav
N Sreedevi
Soumya Vivek
P2860
P356
10.12688/F1000RESEARCH.12102.1
P577
2017-12-21T00:00:00Z