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Medientyp
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Autor/in
- Kutsche, Kerstin
- Abdalla, Ebtesam 2
- Alawi, Malik 2
- Holling, Tess 2
- Altmeppen, Hermann Clemens 1
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4 Einträge gefunden
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Cardiofacioneurodevelopmental syndrome: Report of a novel patient and expansion of the phenotype
2022 - Forschungsinformationssystem des UKE - frei zugänglich -
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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Regulation of Liprin-α phase separation by CASK is disrupted by a mutation in its CaM kinase domain
- Tibbe, Debora
- Ferle, Pia
- Krisp, Christoph
- Nampoothiri, Sheela
- Mirzaa, Ghayda
- Assaf, Melissa
- Parikh, Sumit
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Clinically Relevant KCNQ1 Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca2+ Sensitivity of the Channel
- Bauer, Christiane K
- Holling, Tess
- Horn, Denise
- Laço, Mário Nôro
- Abdalla, Ebtesam
- Omar, Omneya Magdy
- Alawi, Malik