Search

Author/Creator Hirose, Mio

1. A homozygous ABHD16A variant causes a complex hereditary spastic paraplegia with developmental delay, absent speech, and characteristic face. Issue 3 (13th December 2021)

Authors:
Miyake, Noriko; Silva, Sebastián; Troncoso, Mónica; Okamoto, Nobuhiko; Andachi, Yoshiki; Kato, Mitsuhiro; Iwabuchi, Chisato; Hirose, Mio; Fujita, Atsushi; Uchiyama, Yuri; Matsumoto, Naomichi
Journal:
Clinical genetics
Issue:
Volume 101:Issue 3(2022)
Page Start:
359
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search