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Dive into the research topics of 'A PIGN mutation responsible for multiple congenital anomalies-hypotonia-seizures syndrome 1 (MCAHS1) in an Israeli-Arab family'. Together they form a unique fingerprint.- Sort by
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Morad Khayat, Joseph Mark Tilghman, Ilana Chervinsky, Lucia Zalman, Aravinda Chakravarti, Stavit A. Shalev
Research output: Contribution to journal › Article › peer-review