HIGHLIGHTS
- who: TYPE and collaborators from the University of Texas Southwestern Medical Center, United States have published the article: Seipin u2014 still a mysterious protein?, in the Journal: (JOURNAL)
SUMMARY
Seipin mutations have been linked to severe congenital lipodystrophy (BSCL2), motor neuronal disorders and congenital encephalopathy (Magré et_al, 2001; Windpassinger et_al, 2004; Ito and Suzuki, 2009; Guillén-Navarro et_al, 2013). As there are several excellent recent reviews on this topic (e_g (Gao et_al, 2019; Renne et_al, 2020; Rao and Goodman, 2021; Schneiter and Choudhary, 2022), I will focus on most recent insights and . . .
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