Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy - Concepedia

Concepedia

Publication | Open Access

Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy

DOI Full Paper Access

112

Citations

31

References

2016

Year

Mikko Muona, Ryosuke Ishimura, Anni Laari, Yoshinobu Ichimura, Tarja Linnankivi, Riikka Keski‐Filppula, Riitta Herva, Heikki Rantala, Anders Paetau, Minna Pöyhönen,

The American Journal of Human Genetics

Biallelic VariantsGeneticsNeuroscienceSevere Infantile-onset EncephalopathyNeuropathologyMedicine

References

	Year	Citations

Page 1