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Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.
- Source :
-
American Journal of Human Genetics . Dec2021, Vol. 108 Issue 12, p2385-2385. 1p. - Publication Year :
- 2021
- Subjects :
- *ATAXIA
*PEOPLE with epilepsy
*SYNDROMES
Subjects
Details
- Language :
- English
- ISSN :
- 00029297
- Volume :
- 108
- Issue :
- 12
- Database :
- Academic Search Index
- Journal :
- American Journal of Human Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 153783582
- Full Text :
- https://doi.org/10.1016/j.ajhg.2021.11.013