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Entries: 1-4  
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Common pathological mutations in PQBP1 induce nonsense-mediated mRNA decay and enhance exclusion of the mutant exon.
Authors: Musante, Luciana; Kunde, Stella-Amrei; Sulistio, Tina O.; Frints, Suzanna G.M.; Schwartz, Charles E.; Martínez, Francisco; Romano, Corrado; Ropers, Hans-Hilger; Kalscheuer, Vera M.; Fischer, Ute; Grimme, Astrid
Date of Publication (YYYY-MM-DD): 2010-01-01
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 1
Start Page: 90
End Page: 98
Document Type: Article
ID: 533752.0
 
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Untersuchung zur Funktion des PQBP1-Komplexes.
Authors: Kunde, Stella-Amrei
Name of University: Freie Universität Berlin
Place of University: Berlin
Date of Approval (YYYY-MM-DD): 2009
Document Type: PhD-Thesis
ID: 472563.0
Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly
Authors: Shoichet, Sarah A.; Kunde, Stella-Amrei; Viertel, Petra; Schell-Apacik, Can; von Voss, Hubertus; Tommerup, Niels; Ropers, Hans-Hilger; Kalscheuer, Vera M.
Date of Publication (YYYY-MM-DD): 2005-08-17
Title of Journal: Human Genetics
Volume: 117
Issue / Number: 6
Start Page: 536
End Page: 544
Document Type: Article
ID: 271590.0
 
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Molekulargenetische Studien an dem Gen FOXG1B
Authors: Kunde, Stella-Amrei
Type of Thesis (e.g.Diploma): diplom
Date of Approval (YYYY-MM-DD): 2004-11-01
Name of University: Freie Universitaet Berlin
Place of University: Berlin
Document Type: Thesis
ID: 229521.0
 
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Entries: 1-4  
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