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Description
MMDS 1 is caused by mutations in affecting NFU1 and was first identified in three siblings of Mexican origins, while MMDS 2 is the result of a mutation that leads to premature stop codon in the BOLA3 gene causing severe epileptic encephalopathy and elevated lactate and glycine levels

Antioxid Redox Signal 25:6177

Minotti, G

Tetrahedron Lett 59:31573160 Ying YC, Taori K, Kim H, Hong JY, Luesch H (2008) Total synthesis and molecular target of largazole, a histone deacetylase inhibitor

EITC has been found to be a stronger contact sensitizer than PITC in the in vivo model LLNA

Attention UFC athletes
