[HTML][HTML] Case report: A novel APTX p.Ser168GlufsTer19 mutation in a Chinese family with ataxia with oculomotor apraxia type 1
X Wu, N Dong, Z Liu, T Tang, M Liu - Frontiers in Neurology, 2022 - frontiersin.org
Ataxia with oculomotor apraxia type 1 (AOA1) is a rare genetic disorder and is inherited in
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
Case report: A novel APTX p. Ser168GlufsTer19 mutation in a Chinese family with ataxia with oculomotor apraxia type 1
X Wu, N Dong, Z Liu, T Tang, M Liu - Frontiers in Neurology, 2022 - europepmc.org
Ataxia with oculomotor apraxia type 1 (AOA1) is a rare genetic disorder and is inherited in
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
Case report: A novel APTX p. Ser168GlufsTer19 mutation in a Chinese family with ataxia with oculomotor apraxia type 1
X Wu, N Dong, Z Liu, T Tang… - Frontiers in neurology, 2022 - pubmed.ncbi.nlm.nih.gov
Ataxia with oculomotor apraxia type 1 (AOA1) is a rare genetic disorder and is inherited in
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
[HTML][HTML] Case report: A novel APTX p. Ser168GlufsTer19 mutation in a Chinese family with ataxia with oculomotor apraxia type 1
X Wu, N Dong, Z Liu, T Tang, M Liu - Frontiers in Neurology, 2022 - ncbi.nlm.nih.gov
Ataxia with oculomotor apraxia type 1 (AOA1) is a rare genetic disorder and is inherited in
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
Case report: A novel APTX p.Ser168GlufsTer19 mutation in a Chinese family with ataxia with oculomotor apraxia type 1.
X Wu, N Dong, Z Liu, T Tang, M Liu - Frontiers in Neurology, 2022 - europepmc.org
Ataxia with oculomotor apraxia type 1 (AOA1) is a rare genetic disorder and is inherited in
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …
an autosomal recessive manner. It is mainly characterized by childhood-onset progressive …