Items where Author is "Koshimizu, E."
 | Up a level |
Group by: Item Type | No Grouping
Number of items: 2.
(2021) NovelEXOSC9variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy. Journal of Human Genetics. pp. 401-407. ISSN 1434-5161
(2018) A homozygous NOP14 variant is likely to cause recurrent pregnancy loss. Journal of Human Genetics. pp. 425-430. ISSN 1434-5161