IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC)
Source
Stem cell research - ISSN 1873-5061-69 (2023) p. 1-5
Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p. Cys1791Tyr) variant
Source
Stem cell research - ISSN 1873-5061-68 (2023) p. 1-4
IPSC reprogramming of two patients with spondyloepimetaphyseal dysplasia (SEMD, biglycan type)
Source
Stem cell research - ISSN 1873-5061-67 (2023) p. 1-5
A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation
Source
Stem cell research - ISSN 1873-5061-67 (2023) p. 1-4
The genetics and typical traits of thoracic aortic aneurysm and dissection
Source
Annual review of genomics and human genetics - ISSN 1527-8204-23 (2022) p. 223-253