An autosomal dominant ERLIN2 mutation leads to a pure HSP phenotype distinct from the autosomal recessive ERLIN2 mutations (SPG18)

por Park, Jin-Mo, Lee, Byeonghyeon, Kim, Jong-Heun, Park, Seong-Yong, Yu, Jinhoon, Kim, Un-Kyung, Park, Jin-Sung
Publicado 2020