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Homozygous deletion of the entire AAAS gene in a triple A syndrome patient.

Research output: Contribution to journal › Research article › Contributed › peer-review

Contributors

K Koehler - , Department of Paediatrics (First author)
K Hackmann - , Institute of Clinical Genetics (Author)
D Landgraf - (Author)
T Schubert - , Department of Paediatrics, Division of Neuropediatrics (Author)
M Shakiba - (Author)
A Kariminejad - (Author)
A Huebner - , Department of Paediatrics (Author)

Details

Original language	English
Journal	European journal of medical genetics
Publication status	Published - May 2019
Peer-reviewed	Yes

External IDs

PubMed	31071487
Scopus	85065625125

Keywords