Neural tube defect family with recessive trait linked to chromosome 9q21.12-21.31


BAYRİ Y., SÖYLEMEZ B., Seker A., Yuksel Ş. , Tanrikulu B. , ÜNVER O., et al.

CHILDS NERVOUS SYSTEM, cilt.31, ss.1367-1370, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 31 Konu: 8
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1007/s00381-015-2753-z
  • Dergi Adı: CHILDS NERVOUS SYSTEM
  • Sayfa Sayısı: ss.1367-1370

Özet

Meningomyelocele is one of the most common and socioeconomically, psychologically, and physically debilitating neurodevelopmental diseases. A few chromosomal locus and genes have been identified as responsible for the disease; however, clear evidence still needs to be produced. This study aimed to show evidence of a strong genetic linkage in a novel chromosomal locus in a family with this neural tube defect.