Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity

Gelijkaardige items

• The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non‐syndromic mental retardation
  door: Basel‐Vanagaite, L, et al.
  Gepubliceerd in: (2006)
• Assignment of a Novel Locus for Autosomal Recessive Congenital Ichthyosis to Chromosome 19p13.1-p13.2
  door: Virolainen, Elina, et al.
  Gepubliceerd in: (2000)
• Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12–19p13.2
  door: Lyon, Sarah M., et al.
  Gepubliceerd in: (2015)
• Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33
  door: Raza, Muhammad Hashim, et al.
  Gepubliceerd in: (2010)
• Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment
  door: Liaqat, Khurram, et al.
  Gepubliceerd in: (2019)