[HTML][HTML] Ataxia oculomotor apraxia type 1 in the siblings of a family: A novel mutation
P Karimzadeh, SK Kakhki, SSE Nejad… - Iranian journal of …, 2017 - ncbi.nlm.nih.gov
Although AOA1 (ataxia oculomotor apraxia1) is one of the most common causes of
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation
P Karimzadeh, SK Kakhki… - Iranian journal of …, 2017 - pubmed.ncbi.nlm.nih.gov
Although AOA1 (ataxia oculomotor apraxia1) is one of the most common causes of
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
ATAXIA OCULOMOTOR APRAXIA TYPE 1 IN THE SIBLINGS OF A FAMILY: A NOVEL MUTATION
P KARIMZADEH, KS Khayatzadeh, NSS Esmail… - 2017 - sid.ir
Although AOA1 (ataxia oculomotor apraxia1) is one of the most commoncauses of
autosomal recessive cerebellar ataxias in Japanese population, it isreported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it isreported from all over …
Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation.
P Karimzadeh, EN SS, M Houshmand… - Iranian Journal of …, 2017 - europepmc.org
Although AOA1 (ataxia oculomotor apraxia1) is one of the most common causes of
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
Ataxia oculomotor apraxia type 1 in the siblings of a family: a novel mutation.
P Karimzadeh, SK Kakhki, SSE Nejad, M Houshmand… - 2017 - cabidigitallibrary.org
Although AOA1 (ataxia oculomotor apraxia1) is one of the most common causes of
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation
P KARIMZADEH, S KHAYYATZADEH… - Iranian Journal of … - journals.sbmu.ac.ir
Abstract How to Cite This Article: Karimzadeh P, khayatzadeh kakhki S, Esmail Nejad Sh. S.,
Houshmand M, Ghofrani M. Ataxia oculomotor apraxia 1 in two siblings of a family: a novel …
Houshmand M, Ghofrani M. Ataxia oculomotor apraxia 1 in two siblings of a family: a novel …
Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation.
SK KAKHKI, P KARIMZADEH… - Iranian Journal of …, 2017 - search.ebscohost.com
Although AOA1 (ataxia oculomotor apraxia1) is one of the most common causes of
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
ATAXIA OCULOMOTOR APRAXIA TYPE 1 IN THE SIBLINGS OF A FAMILY: A NOVEL MUTATION
P KARIMZADEH, KS Khayatzadeh, NSS Esmail… - 2017 - sid.ir
Although AOA1 (ataxia oculomotor apraxia1) is one of the most commoncauses of
autosomal recessive cerebellar ataxias in Japanese population, it isreported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it isreported from all over …
Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation.
SK KAKHKI, P KARIMZADEH… - Iranian Journal of …, 2017 - search.ebscohost.com
Although AOA1 (ataxia oculomotor apraxia1) is one of the most common causes of
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation
P Karimzadeh, SK Kakhki… - Iranian journal of …, 2017 - pubmed.ncbi.nlm.nih.gov
Although AOA1 (ataxia oculomotor apraxia1) is one of the most common causes of
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …
autosomal recessive cerebellar ataxias in Japanese population, it is reported from all over …