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Diffuse central hypomyelination presenting as 4H syndrome caused by compound heterozygous mutations in POLR3A encoding the catalytic subunit of polymerase III

✍ Scribed by Yasuo Terao; Hirotomo Saitsu; Masaya Segawa; Yukiko Kondo; Kiwako Sakamoto; Naomichi Matsumoto; Shoji Tsuji; Yoshiko Nomura


Book ID
119304573
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
630 KB
Volume
320
Category
Article
ISSN
0022-510X

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