A homozygous loss-of-function mutation in DNAJA3 causes hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V)

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作者：
Kawarai, T.
Miyamoto, R.
Kuroda, Y.
Omoto, M.
Ueyama, M.
Murakami, N.
Furukawa, T.
Oki, R.
Mori, A.
Osaki, Y.
Banzrai, C.
Nodera, H.
Orlacchio, A.
Hashiguchi, A.
Higuchi, Y.
Takashima, H.
Kanda, T.
Izumi, Y.
Nagai, Y.
Mitsui, T.
Kaji, R.
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来源：
MOVEMENT DISORDERS | 2016年 / 31卷
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中图分类号：
R74 [神经病学与精神病学];
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摘要：
955
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页码：S305 / S305
页数：1
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