[HTML][HTML] Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
Background Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
[引用][C] Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
NA Ababneh, D Ali, B Al-Kurdi, M Sallam… - PLoS …, 2020 - ui.adsabs.harvard.edu
Identification of APTX disease-causing mutation in two unrelated Jordanian families with
cerebellar ataxia and sensitivity to DNA damaging agents - NASA/ADS Now on home page …
cerebellar ataxia and sensitivity to DNA damaging agents - NASA/ADS Now on home page …
Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
NA Ababneh, D Ali, B Al-Kurdi, M Sallam, AM Alzibdeh… - PLoS ONE, 2020 - go.gale.com
Autosomal recessive cerebellar ataxias (ARCAs) are clinically and genetically heterogonous
group of disorders [1]. Of these ARCAs, ataxia with oculomotor apraxia type 1 (AOA1) is a …
group of disorders [1]. Of these ARCAs, ataxia with oculomotor apraxia type 1 (AOA1) is a …
[PDF][PDF] Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
NA Ababneh, D Ali, B Al-Kurdi, M Sallam… - PLoS …, 2020 - pdfs.semanticscholar.org
Background Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents.
NA Ababneh, D Ali, B Al-Kurdi, M Sallam, AM Alzibdeh… - Plos one, 2020 - europepmc.org
Background Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
NA Ababneh, D Ali, B Al-Kurdi, M Sallam, AM Alzibdeh… - PLoS ONE, 2020 - lup.lub.lu.se
BACKGROUND: Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal
recessive cerebellar ataxia, caused by mutations in the APTX gene. The disease is …
recessive cerebellar ataxia, caused by mutations in the APTX gene. The disease is …
Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
NA Ababneh, D Ali, B Al-Kurdi, M Sallam… - PLoS …, 2020 - portal.research.lu.se
BACKGROUND: Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal
recessive cerebellar ataxia, caused by mutations in the APTX gene. The disease is …
recessive cerebellar ataxia, caused by mutations in the APTX gene. The disease is …
[HTML][HTML] Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
NA Ababneh, D Ali, B Al-Kurdi, M Sallam… - PLoS ONE, 2020 - ncbi.nlm.nih.gov
Background Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
[PDF][PDF] Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
NA Ababneh, D Ali, B Al-Kurdi, M Sallam… - PLoS ONE, 2020 - researchgate.net
Background Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents.
NA Ababneh, D Ali, B Al-Kurdi, M Sallam… - PLoS …, 2020 - search.ebscohost.com
Background: Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by …