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A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions
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| Zeitschriftentitel: | Frontiers in Genetics |
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| Personen und Körperschaften: | , , , , , , |
| In: | Frontiers in Genetics, 5, 2014 |
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Frontiers Media SA
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Melchionda, Laura Damseh, Nadirah S. Abu Libdeh, Bassam Y. Nasca, Alessia Elpeleg, Orly Zanolini, Alice Ghezzi, Daniele Melchionda, Laura Damseh, Nadirah S. Abu Libdeh, Bassam Y. Nasca, Alessia Elpeleg, Orly Zanolini, Alice Ghezzi, Daniele |
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Melchionda, Laura Damseh, Nadirah S. Abu Libdeh, Bassam Y. Nasca, Alessia Elpeleg, Orly Zanolini, Alice Ghezzi, Daniele |
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Melchionda, Laura Damseh, Nadirah S. Abu Libdeh, Bassam Y. Nasca, Alessia Elpeleg, Orly Zanolini, Alice Ghezzi, Daniele Frontiers in Genetics A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions Genetics (clinical) Genetics Molecular Medicine |
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melchionda, laura |
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Melchionda, Laura Damseh, Nadirah S. Abu Libdeh, Bassam Y. Nasca, Alessia Elpeleg, Orly Zanolini, Alice Ghezzi, Daniele 1664-8021 Frontiers Media SA Genetics (clinical) Genetics Molecular Medicine http://dx.doi.org/10.3389/fgene.2014.00397 A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions Frontiers in Genetics |
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| title |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_unstemmed |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_full |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_fullStr |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_full_unstemmed |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_short |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_sort |
a novel mutation in ttc19 associated with isolated complex iii deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
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Genetics (clinical) Genetics Molecular Medicine |
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http://dx.doi.org/10.3389/fgene.2014.00397 |
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| author | Melchionda, Laura, Damseh, Nadirah S., Abu Libdeh, Bassam Y., Nasca, Alessia, Elpeleg, Orly, Zanolini, Alice, Ghezzi, Daniele |
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| spelling | Melchionda, Laura Damseh, Nadirah S. Abu Libdeh, Bassam Y. Nasca, Alessia Elpeleg, Orly Zanolini, Alice Ghezzi, Daniele 1664-8021 Frontiers Media SA Genetics (clinical) Genetics Molecular Medicine http://dx.doi.org/10.3389/fgene.2014.00397 A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions Frontiers in Genetics |
| spellingShingle | Melchionda, Laura, Damseh, Nadirah S., Abu Libdeh, Bassam Y., Nasca, Alessia, Elpeleg, Orly, Zanolini, Alice, Ghezzi, Daniele, Frontiers in Genetics, A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions, Genetics (clinical), Genetics, Molecular Medicine |
| title | A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_full | A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_fullStr | A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_full_unstemmed | A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_short | A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_sort | a novel mutation in ttc19 associated with isolated complex iii deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| title_unstemmed | A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions |
| topic | Genetics (clinical), Genetics, Molecular Medicine |
| url | http://dx.doi.org/10.3389/fgene.2014.00397 |