Kenji Kurosawa
0000-0002-6817-7748
3 papers found
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MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNAMet gene
Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly
Contiguous gene deletion neighboring TWIST1 identified in a patient with Saethre-Chotzen syndrome associated with neurodevelopmental delay: Possible contribution of HDAC9 : Saethre-Chotzen syndrome
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