ORCID

We notice you are using a browser that our site does not support. Some features on this site may not work correctly. We recommend that you upgrade to a supported browser.

Activities

Collapse all

Identification of novel compound heterozygous mutations in ACO2 in a patient with progressive cerebral and cerebellar atrophy

Molecular Genetics & Genomic Medicine

2019-07 | Journal article

DOI: 10.1002/mgg3.698

Contributors: Masahide Fukada; Keitaro Yamada; Shima Eda; Ken Inoue; Chihiro Ohba; Naomichi Matsumoto; Hirotomo Saitsu; Atsuo Nakayama

Show more detail

Source:

check_circle

Crossref

How many people are using ORCID?