日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome

BAF复合物亚基DPF2的突变与科芬-西里斯综合征相关

Georgia Vasileiou,Silvia Vergarajauregui,Sabine Endele,Bernt Popp,Christian Büttner,Arif B Ekici,Marion Gerard,Nuria C Bramswig,Beate Albrecht,Jill Clayton-Smith,Jenny Morton,Susan Tomkins,Karen Low,Astrid Weber,Maren Wenzel,Janine Altmüller,Yun Li,Bernd Wollnik,George Hoganson,Maria-Renée Plona,Megan T Cho

Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy

描述 SPTAN1 相关表型:从孤立性癫痫到伴有进行性脑萎缩的脑病

Steffen Syrbe, Frederike L Harms, Elena Parrini, Martino Montomoli, Ulrike Mütze, Katherine L Helbig, Tilman Polster, Beate Albrecht, Ulrich Bernbeck, Ellen van Binsbergen, Saskia Biskup, Lydie Burglen, Jonas Denecke, Bénédicte Heron, Henrike O Heyne, Georg F Hoffmann, Frauke Hornemann, Takeshi Mats

Mutations affecting the BHLHA9 DNA-binding domain cause MSSD, mesoaxial synostotic syndactyly with phalangeal reduction, Malik-Percin type

影响 BHLHA9 DNA 结合域的突变会导致 MSSD、伴有指骨缩小的中轴骨性并指畸形、Malik-Percin 型

Sajid Malik, Ferda E Percin, Dorothea Bornholdt, Beate Albrecht, Antonio Percesepe, Manuela C Koch, Antonio Landi, Barbara Fritz, Rizwan Khan, Sara Mumtaz, Nurten A Akarsu, Karl-Heinz Grzeschik

Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome--an autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13

埃勒斯-丹洛斯综合征的脊椎关节发育不良症——由锌转运蛋白基因 SLC39A13 突变引起的常染色体隐性遗传疾病

Cecilia Giunta, Nursel H Elçioglu, Beate Albrecht, Georg Eich, Céline Chambaz, Andreas R Janecke, Heather Yeowell, MaryAnn Weis, David R Eyre, Marius Kraenzlin, Beat Steinmann