Whole-exome sequencing identifies a de novo TUBA1A mutation in a patient with sporadic malformations of cortical development: a case report (Q33988618)
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English | Whole-exome sequencing identifies a de novo TUBA1A mutation in a patient with sporadic malformations of cortical development: a case report |
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Whole-exome sequencing identifies a de novo TUBA1A mutation in a patient with sporadic malformations of cortical development: a case report (English)
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Keiko Shimojima
Aya Narita
Yoshihiro Maegaki
Akira Saito
Toshiyuki Yamamoto
22 July 2014
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