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X连锁脑积水家族中L1CAM基因的五个新突变。

Five novel mutations in the L1CAM gene in families with X linked hydrocephalus.

作者信息

Gu S M, Orth U, Veske A, Enders H, Klunder K, Schlosser M, Engel W, Schwinger E, Gal A

机构信息

Institut fur Humangenetik, Medizinische Universitat zu Lubeck, Germany.

出版信息

J Med Genet. 1996 Feb;33(2):103-6. doi: 10.1136/jmg.33.2.103.

Abstract

Five novel mutations have been identified in the gene encoding L1CAM, a neural cell adhesion protein, in families with X linked hydrocephalus (XHC). Interestingly, all five mutations are in the evolutionarily highly conserved Ig-like domains of the protein. The two frameshift mutations (52insC and 955delG) and the nonsense mutation (Trp276Ter) most probably result in functional null alleles and complete absence of L1CAM at the cell surface. The two missense mutations (Tyr194Cys and Pro240Leu) may considerably alter the structure of the L1CAM protein. These data provide convincing evidence that XHC is genetically extremely heterogeneous.

摘要

在患有X连锁脑积水(XHC)的家族中,已在编码神经细胞粘附蛋白L1CAM的基因中鉴定出五个新突变。有趣的是,所有五个突变都位于该蛋白质进化上高度保守的免疫球蛋白样结构域中。两个移码突变(52insC和955delG)和无义突变(Trp276Ter)很可能导致功能性无效等位基因,并使细胞表面完全不存在L1CAM。两个错义突变(Tyr194Cys和Pro240Leu)可能会极大地改变L1CAM蛋白的结构。这些数据提供了令人信服的证据,表明XHC在遗传上极其异质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9ce/1051833/41accb420eb5/jmedgene00256-0017-a.jpg

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