Sca1+ Stem Cell Survival and Engraftment in the Infarcted Heart Circulation

Sca1+ Stem Cell Survival and Engraftment in the Infarcted Heart Circulation. Diseases associated with atxn1 include spinocerebellar ataxia 1 and primary cerebellar. 161 rows genecards summary for atxn1 gene.

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Description category gifts gc id. Summaries for scaant1 gene genecards summary for scaant1 gene scaant1 (sca7/atxn7 antisense rna 1) is an rna gene, and is affiliated with the lncrna class. Diseases associated with cav1 include lipodystrophy, congenital generalized, type 3 and pulmonary hypertension, primary, 3.

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Spinocerebellar ataxia type 1 (sca 1) is an autosomal dominant disorder characterized by neurodegeneration of the cerebellum, spinal cord and brainstem. In disease pathogenesis, polyglutamine expansion.

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Atxn1 (ataxin 1) is a protein coding gene. Spinocerebellar ataxia type 1 (sca1) is a rare autosomal dominant disorder, which, like other spinocerebellar ataxias, is characterized by neurological symptoms including dysarthria,.

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Diseases associated with atxn1 include spinocerebellar ataxia 1 and primary cerebellar. Spinocerebellar ataxia type 1 (sca 1) is an autosomal dominant disorder characterized by neurodegeneration of the cerebellum, spinal cord and brainstem.

Atxn1 (Ataxin 1) Is A Protein Coding Gene.

Spinocerebellar ataxia type 1 (sca1) is a rare autosomal dominant disorder, which, like other spinocerebellar ataxias, is characterized by neurological symptoms including dysarthria,. Cav1 (caveolin 1) is a protein coding gene. Diseases associated with cav1 include lipodystrophy, congenital generalized, type 3 and pulmonary hypertension, primary, 3.

Diseases Associated With Atxn1 Include Spinocerebellar Ataxia 1 And Primary Cerebellar.

161 rows genecards summary for atxn1 gene. Spinocerebellar ataxia type 1 (sca 1) is an autosomal dominant disorder characterized by neurodegeneration of the cerebellum, spinal cord and brainstem. Identification of the specific gene.

Summaries For Scaant1 Gene Genecards Summary For Scaant1 Gene Scaant1 (Sca7/Atxn7 Antisense Rna 1) Is An Rna Gene, And Is Affiliated With The Lncrna Class.

Description category gifts gc id. Spinocerebellar ataxia 1 is an autosomal dominant disease characterized by neurodegeneration and motor dysfunction. In disease pathogenesis, polyglutamine expansion.