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Paper Details

Bi-allelic loss-of-function variants in <i>KIF21A</i> cause severe fetal akinesia with arthrogryposis multiplex.
J Med Genet
24
2023
FA, Fetal akinesia, KIF21A, Kif21a, arthrogryposis, arthrogryposis multiplex, arthrogryposis of multiple joints, disease genes, disease loci, facial dysmorphisms, fetal akinesia, kinesin family member 21A gene, neurogenic FA sequence, piglets, pulmonary hypoplasia
Author NameAffiliation
Petra St??beInstitute of Medical Genetics and Applied Genomics, University of Tuebingen
Denise HornInstitute of Medical and Human Genetics, Charite - Universitatsmedizin Berlin
Reiner SiebertInstitute of Human Genetics, Ulm University and Ulm University Medical Center
Stephan OssowskiInstitute of Medical Genetics and Applied Genomics, University of Tuebingen
Andreas DufkeInstitute of Medical Genetics and Applied Genomics, University of Tuebingen
Andreas DufkeUniversity of Tuebingen
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