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The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration.
Schwenty-Lara, Janina; Nehl, Denise; Borchers, Annette.
Affiliation
  • Schwenty-Lara J; Department of Biology, Molecular Embryology, Philipps-Universität Marburg, Marburg 35043, Germany.
  • Nehl D; Department of Biology, Molecular Embryology, Philipps-Universität Marburg, Marburg 35043, Germany.
  • Borchers A; Department of Biology, Molecular Embryology, Philipps-Universität Marburg, Marburg 35043, Germany.
Hum Mol Genet ; 29(2): 305-319, 2020 01 15.
Article in En | MEDLINE | ID: mdl-31813957
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Vestibular Diseases / Histone-Lysine N-Methyltransferase / Xenopus Proteins / Face / Hematologic Diseases / Neural Crest Type of study: Prognostic_studies Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Vestibular Diseases / Histone-Lysine N-Methyltransferase / Xenopus Proteins / Face / Hematologic Diseases / Neural Crest Type of study: Prognostic_studies Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Country of publication: