A reply to a commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness
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Veröffentlicht in: | Journal of human genetics 2015-03, Vol.60 (3), p.163-164 |
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container_title | Journal of human genetics |
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creator | Yim, Shin-Young Jeong, Seon-Yong |
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doi_str_mv | 10.1038/jhg.2014.119 |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature - Complete Springer Journals |
subjects | Children Epilepsy Epilepsy - genetics Female Humans Intellectual disabilities Intellectual Disability - genetics Male Muscle Proteins - genetics Muscle Weakness - genetics |
title | A reply to a commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness |
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