Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A - Concepedia

Concepedia

Publication | Open Access

Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A

DOI Full Paper Access

45

Citations

46

References

2019

Year

Feifei Tao, Gary W. Beecham, Adriana Rebelo, John Svaren, Susan H. Blanton, John J. Moran, Camila Lopez‐Anido, Jasper M. Morrow, Lisa Abreu, Devon Rizzo,

Annals of Neurology

Abstract

SIPA1L2 is a potential genetic modifier of CMT1A phenotypic expressions and offers a new pathway to therapeutic interventions. ANN NEUROL 2019;85:316-330.

References

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