Case report: prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in gene

HIGHLIGHTS

• who: JAM and collaborators from the Hebei Normal University, China have published the Article: Case report: Prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in gene, in the Journal: (JOURNAL)
• what: Our investigation identified the compound heterozygous variants of c.712 + 2T > A and c.813C > G in the frontiersin.org 10.3389/fgene.2022.1036231
• how: The compound variants of c.712 + 2T > A and c.813C > G p.Tyr271* were identified in the JAM3 (NM_032801.4) gene both in the proband (II 2) and his brother (II 3) neither . . .
  

   

  

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