Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation.

Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation. Clin Genet. 2019 Jul 08;: Authors: Faruq M, Kumar D, Wadhwa S, Shamim U, Mathur A, Parveen S, Garg A, Srivastava AK PMID: 31286494 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31286494?dopt=Abstract

Source: Clinical Genetics - July 7, 2019 Category: Genetics & Stem Cells Authors: Faruq M, Kumar D, Wadhwa S, Shamim U, Mathur A, Parveen S, Garg A, Srivastava AK Tags: Clin Genet Source Type: research

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