Genotype-phenotype study and expansion of ARL6IP1-related complicated hereditary spastic paraplegia.

Genotype-phenotype study and expansion of ARL6IP1-related complicated hereditary spastic paraplegia. Clin Genet. 2020 Nov 13;: Authors: Cao Y, Manning M, Pope K, He W, Vetrini F, Siskind C, Rosenfeld JA, Yang Y, Xiao R PMID: 33188530 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/33188530?dopt=Abstract

Source: Clinical Genetics - November 13, 2020 Category: Genetics & Stem Cells Authors: Cao Y, Manning M, Pope K, He W, Vetrini F, Siskind C, Rosenfeld JA, Yang Y, Xiao R Tags: Clin Genet Source Type: research

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