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Dive into the research topics of 'Variation in SIPA1L2 is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A'. Together they form a unique fingerprint.- Sort by
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Variation in SIPA1L2 is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A
for the Inherited Neuropathy Consortium
Research output: Contribution to journal › Article › peer-review
13
Scopus
citations