Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

H Date, O Onodera, H Tanaka, K Iwabuchi, K Uekawa… - Nature …, 2001 - nature.com
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative
disease among Europeans and people of European descent, is characterized by an early …
被引用次数：428 相关文章

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.

O Onodera, H Tanaka, K Iwabuchi… - Nature …, 2001 - search.ebscohost.com
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative
disease among Europeans and people of European descent, is characterized by an early …

[引用][C] Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

O ONODERA, T SAKAI, T TAKAHASHI… - Nature …, 2001 - pascal-francis.inist.fr
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations
in a new HIT superfamily gene CNRS Inist Pascal-Francis CNRS Pascal and Francis …

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.

O Onodera, H Tanaka, K Iwabuchi, K Uekawa… - Nature …, 2001 - europepmc.org
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative
disease among Europeans and people of European descent, is characterized by an early …

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

H Date, O Onodera, H Tanaka, K Iwabuchi… - Nature …, 2001 - go.gale.com
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative
disease among Europeans and people of European descent, is characterized by an early …

[引用][C] Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

H Date, O Onodera, H Tanaka, K Iwabuchi, K Uekawa… - Nature Genetics, 2001 - cir.nii.ac.jp
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations
in a new HIT superfamily gene | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

H Date, O Onodera, H Tanaka, K Iwabuchi… - Nature …, 2001 - pubmed.ncbi.nlm.nih.gov
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative
disease among Europeans and people of European descent, is characterized by an early …

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.

O Onodera, H Tanaka, K Iwabuchi, K Uekawa… - Nature …, 2001 - europepmc.org
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative
disease among Europeans and people of European descent, is characterized by an early …

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.

O Onodera, H Tanaka, K Iwabuchi… - Nature …, 2001 - search.ebscohost.com
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative
disease among Europeans and people of European descent, is characterized by an early …

[引用][C] Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

H DATE, O ONODERA, H TANAKA… - Nature …, 2001 - Nature Publishing Group