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Article

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

Clinical genetics - 1 Mar 2021

Cao Ye, Manning Melanie, Pope Kathleen, He Weimin, Vetrini Francesco, Siskind Carly, Rosenfeld Jill A, Yang Yaping, Xiao Rui

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Share to Adaptor Proteins, Signal Transducing
Share to Exome Sequencing
Share to Fatal Outcome
Share to Genetic Association Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Loss of Function Mutation

Share to Membrane Proteins

Share to Mutation, Missense

Share to Spastic Paraplegia, Hereditary

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Identifiers

PMID: 33188530
DOI: 10.1111/cge.13870

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