Disease‐Causing Variants in the ATL1 Gene Are a Rare Cause of Hereditary Spastic Paraplegia among Czech Patients

No abstract is available for this paper.

• Publication year

  2017

• Venue

  Annals of Human Genetics

• Publication date

  2017-07-24

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1111/ahg.12206PMID 28736820
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Extensive In Silico Analysis of ATL1 Gene : Discovered Five Mutations That May Cause Hereditary Spastic Paraplegia Type 3A

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