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Paper Details

Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency.
Hum Mol Genet
4
2022
HOX gene, HOXA1, HOXA4, HOXA7, HOXB2, KMT2 family, KMT2D, Kabuki syndrome, RNA, Suleiman-El-Hattab syndrome, TASP1, TASP1 deficiency, TASP1 loss-of-function variants, TFIIA complex, Wiedemann-Steiner and Kabuki syndrome, Zebrafish, Zebrafish tasp1, blood, cardiovascular and posterior fossa malformations, congenital anomalies, developmental delay, fibroblasts, histone, histone methyltransferases, histone modification disorder, neurodevelopmental syndrome, tasp1, tasp1 orthologue, transcription factor TFIIA, zebrafish
Author NameAffiliation
Anne SlavotinekUniversity of California san francisco
Anne SlavotinekUniversity of California san francisco
Thomas MeitingerInstitute of Human Genetics, Technical University of Munich
Thomas MeitingerInstitute of Human Genetics, Technical University of Munich
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