Concepedia

Publication | Closed Access

Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction

DOI

16

Citations

6

References

2018

Year

Mara Cavallin, Amandine Béry, Camille Maillard, Laurent Salomon, Christine Bole, Madeline Louise Reilly, Patrick Nitschké, Nathalie Boddaert, Nadia Bahi‐Buisson
European Journal of Medical Genetics

References

YearCitations

Page 1