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Novel frameshift variant of NHLRC1 gene in compound heterozygosity in an adult Greek patient with Lafora disease
被引:1
|作者:
Afrantou, Theodora
[1
]
Lagoudaki, Roza
[1
]
Papadopoulos, Theofanis
[2
]
Karayannopoulou, Georgia
[3
]
Galidis, Eleftherios
[3
]
Migkos, Konstantinos
[1
]
Stavridou, Eleni
[1
]
Kimiskidis, Vasilios
[4
]
Ioannidis, Panagotis
[1
]
Grigoriadis, Nikolaos
[1
]
机构:
[1] Aristotle Univ Thessaloniki, Ahepa Univ Hosp, B Dept Neurol, Stilp Kyriakidis 1, Thessaloniki 54636, Greece
[2] Lab Mol Biol & Genet Karyo Ltd, Thessaloniki, Greece
[3] Aristotle Univ Thessaloniki, Ahepa Univ Hosp, Dept Pathol, Thessaloniki, Greece
[4] Aristotle Univ Thessaloniki, Ahepa Univ Hosp, Clin Neurophysiol Lab, Thessaloniki, Greece
来源:
关键词:
Novel frameshift variant;
NHLRC1;
gene;
Compound heterozygosity;
Lafora disease;
Progressive myoclonus epilepsy;
Drug resistant epilepsy;
MUTATION;
D O I:
10.1016/j.seizure.2021.01.011
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
[No abstract available]
引用
收藏
页码:49 / 51
页数:3
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