https://www.selleckchem.com/Androgen-Receptor.html
All the mutations were located within KIF1A motor domain. Six cases had pure phenotypes, of which 5 were familial, where 2 familial cases demonstrated incomplete penetrance, early onset and slow relatively benign SPG course. All 4 complicated cases were caused by novel mutations without familial history. The phenotypes varied from severe in two patients (e.g. lack of walking, pronounced mental retardation) to relatively mild non-disabling symptoms in two others. AD SPG30 is one of the most common forms of SPG in Russia, the disorder ha
Curtir
Comentario
Compartilhar
