HOMOZYGOUS VARIANTS IN ATP1A2 CAUSE A NEW LETHAL SYNDROME OF RENATAL HYDROPS, MICROCEPHALY, CORTICAL MALFORMATIONS, AND CONTRACTURES-A REPORT OF THREE FAMILIES

C. J. Curry, F. P. Monteiro, E. Hobson, I. Berry,R. Hevner, J. H. Fisher, J. Turocy,A. Vetro,W. B. Dobyns

AMERICAN JOURNAL OF MEDICAL GENETICS PART A(2020)

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