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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

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