Zobrazeno 1 - 1
of 1
pro vyhledávání: '"mitochondrial dna depletion syndrome type 7(hepatocerebral type)"'
Publikováno v:
罕见病研究, Vol 3, Iss 3, Pp 329-334 (2024)
This study presents a case of a girl of three year and 4 month old with ataxia and severe sensorineural hearing loss for 2 years. In order to improve hearing, she was hospitalized in the PUMC Hospital. Genetic testing performed found compound heteroz
Externí odkaz:
https://doaj.org/article/47f1074dcd9a4689ae66726da306e342