FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects - Concepedia

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FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects

DOI Full Paper Access

13

Citations

25

References

2022

Year

Auriane Cospain, Ana Rivera‐Barahona, Erwan Dumontet, Blanca Gener, Isabelle Bailleul‐Forestier, Isabelle Meyts, Guillaume Jouret, Bertrand Isidor, Carole Brewer, Wim Wuyts,

Genetics in Medicine

Last Exon CauseDevelopmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsEnamel DefectsCraniofacial DevelopmentNeuroscienceAbnormal DevelopmentMedicineNeurogenetics

References

	Year	Citations

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