Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia

T Kato, Y Tamura, H Matsumoto, O Kobayashi… - Clinical …, 2021 - Elsevier
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH) is a
neurodegenerative disorder caused by mutation in the aprataxin (APTX)-coding gene APTX …
被引用次数：2 相关文章

Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia.

T Kato, Y Tamura, H Matsumoto… - Clinical Immunology …, 2021 - europepmc.org
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH) is a
neurodegenerative disorder caused by mutation in the aprataxin (APTX)-coding gene APTX …

Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia

T Kato, Y Tamura, H Matsumoto… - Clinical …, 2021 - pubmed.ncbi.nlm.nih.gov
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH) is a
neurodegenerative disorder caused by mutation in the aprataxin (APTX)-coding gene APTX …

[引用][C] Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia

T Kato, Y Tamura, H Matsumoto, O Kobayashi… - Clinical …, 2021 - cir.nii.ac.jp
Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia
and hypoalbuminemia | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] …