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AFG3L2 Polyclonal Antibody, 100ul Drug Development and Evaluation Molecular cloning and analysis of

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AFG3L2 Polyclonal Antibody, 100ul Drug Development and Evaluation Molecular cloning and analysis ofThis gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.

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Description

Molecular cloning and analysis of several PSG genes has indicated that the PSGs form a subgroup of the carcinoembryonic antigen (CEA) gene family

3)-fucosyltransferase and alpha(1

The protein encoded by this gene is most closely related to HUS1

The centromeric copy may be a modifier of disease caused by mutation in the telomeric copy

GSC2 is expressed in a limited number of adult tissues

AFG3L2 Polyclonal Antibody, 100ul Drug Development and Evaluation Molecular cloning and analysis ofThis gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.

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