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Journal of Medical Genetics, ISSN 0022-2593, 2018, Volume 56, Issue 5, p. 332
Putative nucleotidyltransferase MAB21L1 is a member of an evolutionarily well-conserved family of the male abnormal 21 (MAB21)-like proteins. Little is known... 
corneal dystrophy | Cerebello-Oculo-Facio-genital (COFG) syndrome | MAB21L1 | pontocerebellar hypoplasia | scrotal/labial aplasia
Journal Article
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 3, pp. 457 - 464
Journal Article
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