Facetten
Zugriff
Einrichtung
Medientyp
- Text 3
Karte
Erscheinungsjahr
Autor/in
- Johannsen, Jessika
- Kutsche, Kerstin
- Bierhals, Tatjana 2
- Altmeppen, Hermann Clemens 1
- Campiglio, Marta 1
- alle zeigen
Sprache
- Englisch 3
3 Einträge gefunden
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Autosomal dominantly inherited myopathy likely caused by the TNNT1 variant p.(Asp65Ala)
- Holling, Tess
- Lisfeld, Jasmin
- Johannsen, Jessika
- Matschke, Jakob
- Song, Feizhi
- Altmeppen, Hermann Clemens
- Kutsche, Kerstin
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A homozygous missense variant in CACNB4 encoding the auxiliary calcium channel beta4 subunit causes a severe neurodevelopmental disorder and impairs channel and non-channel functions
- Coste de Bagneaux, Pierre
- von Elsner, Leonie
- Bierhals, Tatjana
- Campiglio, Marta
- Johannsen, Jessika
- Obermair, Gerald J
- Hempel, Maja
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Biallelic variants in SMAD6 are associated with a complex cardiovascular phenotype
- Kloth, Katja
- Bierhals, Tatjana
- Johannsen, Jessika
- Harms, Frederike L
- Juusola, Jane
- Johnson, Mark C
- Grange, Dorothy K