All individuals with variants in gene ISCA1

2 entries on 1 page. Showing entries 1 - 2.
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00248822 Fam1P1/P2 PubMed: Shukla 2017 2-generation family, affected sister/brother, unaffected heterozygous carrier parents F;M yes India - - - - - MMDS see paper; ..., early onset neurological deterioration, seizures, extensive white matter abnormalities, cortical migrational abnormalities, lactic acidosis, early demise 1 2 Johan den Dunnen
00248823 Fam2PatP3/P4 PubMed: Shukla 2017 2-generation family, affected brother/sister, unaffected heterozygous carrier parents F;M no India - - - - - MMDS see paper; ..., early onset neurological deterioration, seizures, extensive white matter abnormalities, cortical migrational abnormalities, lactic acidosis, early demise 1 2 Johan den Dunnen
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