EXOSC9 mutation causes pontocerebellar hypoplasia type 1D (PCH1D): Refining the phenotype and literature review

التفاصيل البيبلوغرافية
العنوان: EXOSC9 mutation causes pontocerebellar hypoplasia type 1D (PCH1D): Refining the phenotype and literature review
المؤلفون: Hossein Jafari Khamirani, Ali Saber Sichani, Seyed Mehdi Panahandeh, Sina Zoghi, Seyed Sajjad Tabei, Maryam Darayee, Mahdieh Talebzadeh, Mehdi Dianatpour, Seyed Alireza Dastgheib, Seyed Mohammad Bagher Tabei
المصدر: Gene Reports. 27:101568
بيانات النشر: Elsevier BV, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Genetics
تدمد: 2452-0144
DOI: 10.1016/j.genrep.2022.101568
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5998d31158f56a5e11517d00411f3d77
https://doi.org/10.1016/j.genrep.2022.101568
Rights: CLOSED
رقم الانضمام: edsair.doi...........5998d31158f56a5e11517d00411f3d77
قاعدة البيانات: OpenAIRE
الوصف
تدمد:24520144
DOI:10.1016/j.genrep.2022.101568