{Reference Type}: Journal Article
{Title}: A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signs.
{Author}: Mascaro M;D'Ambrosio L;Lazzari E;Almoguera B;Swafiri ST;Zanchetta ME;Meroni G;
{Journal}: Biochim Biophys Acta Mol Basis Dis
{Volume}: 1870
{Issue}: 4
{Year}: 2024 Apr 18
{Factor}: 6.633
{DOI}: 10.1016/j.bbadis.2024.167126