Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay

Mindy H. Li*, Kelly Arndt, Soma Das, Elliott M. Weiss, Yaning Wu, Kriti Gwal, Karuna V. Shekdar, Elaine H. Zackai

*Corresponding author for this work

Research output: Contribution to journal › Letter › peer-review

4 Scopus citations

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