Affiner les résultats
Type de document
Institution
Collection spécifique
Langue
- Anglais (2)
Auteur
- Lochmüller, Hanns (2)
- Abicht, Angela (1)
- Briguet, Alexandre (1)
- Brodherr, Turgut (1)
- Bruchertseifer, Vera (1)
- Eger, Katharina (1)
- Fischer, Dirk (1)
- Fürst, Dieter O. (1)
- Germing, Alfried (1)
- Hellenbroich, Yorck (1)
- Heyer, Christoph M. (1)
- Huebner, Angela (1)
- Höpfner, Sebastian (1)
- Ketelsen, Uwe-Peter (1)
- Kirschner, Janbernd (1)
- Kley, Rudolf A. (1)
- Müller, Klaus (1)
- Müller‐Felber, Wolfgang (1)
- Peters, Sören A. (1)
- Pongratz, Dieter (1)
- Reum, Conny (1)
- Ruegg, Markus A. (1)
- Schmidt, Carolin (1)
- Schröder, Rolf (1)
- Song, In‐Ho (1)
- Stucka, Rolf (1)
- Tolksdorf, Karen (1)
- Vorgerd, Matthias (1)
- Walter, Maggie C. (1)
- van der Ven, Peter F. M. (1) Plus Moins
Mot clé
- AChRϵ = epsilon subunit of the acetylcholine receptor (1)
- Abbreviations: AChR = acetylcholine receptor (1)
- CMS = congenital myasthenic syndrome (1)
- FLNC mutation (1)
- Keywords: acetylcholine receptor (1)
- Original Articles (1)
- RACE = rapid amplification of cDNA ends (1)
- RT-PCR = reverse transcription PCR (1)
- SNP = single nucleotide polymorphism (1)
- bp = base pair (1)
- congenital myasthenic syndrome (1)
- epsilon subunit (1)
- filamin C (1)
- gene deletion (1)
- kb = kilobase pair (1)
- mt = mutant (1)
- muscular dystrophy (1)
- myofibrillar myopathy (1)
- phenotype (1)
- promoter mutation (1)
- wt = wild type (1) Plus Moins