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A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder
PaperCitations, authors & open-access status
A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 33 citations, 2011 year and closed oa status.
33
Citations
2011
Year
closed
OA Status