Report of a novel missense TDP1 variant in a Pakistani family affected with an extremely rare disorder congenital spinocerebellar ataxia with axonal neuropathy type 1 (SCAN1)

Authors

Riaz Ahmad

Published

November 22, 2024

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Journal

Molecular Biology Reports

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DOI

10.1007/s11033-024-10085-8

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Report of a novel missense TDP1 variant in a Pakistani family affected with an extremely rare disorder congenital spinocerebellar ataxia with axonal neuropathy type 1 (SCAN1)

Authors

Riaz Ahmad

Published

November 22, 2024

Add a comment...

Supporters

Support the authors with ResearchCoin

Journal

Molecular Biology Reports

Topics

DOI

10.1007/s11033-024-10085-8

License

CC-BY

Paper

Paper

Paper

Paper

Report of a novel missense TDP1 variant in a Pakistani family affected with an extremely rare disorder congenital spinocerebellar ataxia with axonal neuropathy type 1 (SCAN1)

Supporters

Journal

Topics

DOI

License

Report of a novel missense TDP1 variant in a Pakistani family affected with an extremely rare disorder congenital spinocerebellar ataxia with axonal neuropathy type 1 (SCAN1)

Supporters

Journal

Topics

DOI

License

Supporters

Journal

Topics

DOI

License