Hypotonia, Ataxia, and Delayed Development Syndrome caused by the EBF3 mutation in a Korean boy with muscle hypotonia

Autor:	Go Hun Seo, Yoon-Ha Choi, Beom Hee Lee, Yena Lee, Tae-Gyeong Kim, Minji Kang
Rok vydání:	2020
Předmět:	Pediatrics medicine.medical_specialty Muscle Hypotonia Ataxia business.industry Mutation (genetic algorithm) medicine medicine.symptom business Hypotonia
Zdroj:	Journal of Genetic Medicine. 17:92-96
ISSN:	2383-8442 1226-1769
DOI:	10.5734/jgm.2020.17.2.92
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::be33dae7418f776addeb6420fbf80547 https://doi.org/10.5734/jgm.2020.17.2.92 Zobrazit plný text záznamu