Biallelic POLR3A variants cause Wiedemann-Rautenstrauch syndrome with atypical brain involvement

Detalles Bibliográficos
Autores principales: Moon, Byungseung, Kim, Minhye, Kim, Hye Jin, Cho, Jae So, Son, Hey Joon, Lim, Byung Chan, Kim, Ki Joong, Chae, Jong Hee, Kim, Soo Yeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Pediatric Society 2022
Materias:
Clinical Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989718/
https://www.ncbi.nlm.nih.gov/pubmed/36596744
http://dx.doi.org/10.3345/cep.2022.01144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989718/
https://www.ncbi.nlm.nih.gov/pubmed/36596744
http://dx.doi.org/10.3345/cep.2022.01144

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