[HTML][HTML] Ataxia with oculomotor apraxia type 1 associated with mutation in the APTX gene: A case study and literature review
R Albaradie, A Alharbi, G Alsaffar… - Experimental and …, 2022 - spandidos-publications.com
Cerebellar ataxia is a disorder characterized by a broad spectrum of phenotypes. Ataxia with
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
[HTML][HTML] Ataxia with oculomotor apraxia type 1 associated with mutation in the APTX gene: A case study and literature review
R Albaradie, A Alharbi, G Alsaffar… - Experimental and …, 2022 - ncbi.nlm.nih.gov
Cerebellar ataxia is a disorder characterized by a broad spectrum of phenotypes. Ataxia with
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
Ataxia with oculomotor apraxia type 1 associated with mutation in the APTX gene: A case study and literature review
A Alharbi, G Alsaffar, B Alhamad… - Experimental and …, 2022 - search.proquest.com
Cerebellar ataxia is a disorder characterized by a broad spectrum of phenotypes. Ataxia with
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
Ataxia with oculomotor apraxia type 1 associated with mutation in the APTX gene: A case study and literature review
R Albaradie, A Alharbi, G Alsaffar… - Experimental and …, 2022 - europepmc.org
Cerebellar ataxia is a disorder characterized by a broad spectrum of phenotypes. Ataxia with
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
Ataxia with oculomotor apraxia type 1 associated with mutation in the APTX gene: A case study and literature review.
R Albaradie, A Alharbi, G Alsaffar… - Experimental & …, 2022 - search.ebscohost.com
Cerebellar ataxia is a disorder characterized by a broad spectrum of phenotypes. Ataxia with
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
Ataxia with oculomotor apraxia type 1 associated with mutation in the APTX gene: A case study and literature review
R Albaradie, A Alharbi, G Alsaffar… - Experimental and …, 2022 - pubmed.ncbi.nlm.nih.gov
Cerebellar ataxia is a disorder characterized by a broad spectrum of phenotypes. Ataxia with
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
Ataxia with oculomotor apraxia type 1 associated with mutation in the APTX gene: A case study and literature review.
R Albaradie, A Alharbi, G Alsaffar… - Experimental and …, 2022 - europepmc.org
Cerebellar ataxia is a disorder characterized by a broad spectrum of phenotypes. Ataxia with
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …