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Medientyp
- Text 3
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Erscheinungsjahr
Autor/in
- Kutsche, Kerstin
- Alawi, Malik 2
- Abdollahpour, Hengameh 1
- Beckstette, Michael 1
- Brand, Kristina 1
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Sprache
- Englisch 3
3 Einträge gefunden
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An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome
- Abdollahpour, Hengameh
- Alawi, Malik
- Kortüm, Fanny
- Beckstette, Michael
- Seemanova, Eva
- Komárek, Vladimír
- Rosenberger, Georg
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Mutations in NDUFB11, Encoding a Complex I Component of the Mitochondrial Respiratory Chain, Cause Microphthalmia with Linear Skin Defects Syndrome
- van Rahden, Vanessa A
- Fernandez-Vizarra, Erika
- Alawi, Malik
- Brand, Kristina
- Fellmann, Florence
- Horn, Denise
- Zeviani, Massimo
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