NGS of 9 gene panel: COX7B, GFM2, NUP62, RARS2, SLC19A2, SLC19A3, SLC25A12, SLC25A19, TPK1

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Documentation:
Ref: LV3262 Categories: , , , , , , , Diseases: Thiamine metabolism dysfunction syndromes and Microcephaly.Genes: SLC25A12, SLC19A2, SLC25A19, COX7B, SLC19A3, RARS2, GFM2, TPK1, NUP62Delivery term: 42 days
sistemas genómicos
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