Concepedia

Publication | Open Access

A recurrent <i>PJA1</i> variant in trigonocephaly and neurodevelopmental disorders

DOIFull Paper Access

28

Citations

43

References

2020

Year

Toshimitsu Suzuki, Toshifumi Suzuki, Matthieu Raveau, Noriko Miyake, Genki Sudo, Yoshinori Tsurusaki, Takaki Watanabe, Yuki Sugaya, Tetsuya Tatsukawa, Emi Mazaki,
Annals of Clinical and Translational Neurology

Abstract

These findings propose novel candidate genes including PJA1 and MSX2 for NDDs associated with craniofacial abnormalities and/or epilepsy.

References

YearCitations

Page 1