A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder
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 PICO Portal from OpenAlex.
How many citations does A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder have?
A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder has 33 citations in the OpenAlex counts PICO Portal stores.
When was A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder published?
A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder has 2011 year in the PICO Portal index.
What is the open-access status of A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder?
A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder has closed oa status in the PICO Portal index.
What is the DOI of A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder?
The DOI for A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder is on the source record.
What is the PMID of A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder?
The PMID for A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder is on the source record.
What is the OpenAlex record for A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder?
The OpenAlex for A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder is on the source record.