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May 22, 2000Human Molecular GeneticsOpen Access

Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene

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MVMark VeugelersBrigham and Women's Hospital

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Mark Veugelers (2000) studied this question.

synapsesocial.com/papers/6a092c8fa419c5e264d2622fhttps://doi.org/10.1093/hmg/9.9.1321
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A small interstitial deletion in the GPC3 gene causes Simpson-Golabi-Behmel syndrome in a Dutch-Canadian family1999 · 49 citations
  2. 2Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome1998 · 187 citations
  3. 3The division abnormally delayed (dally) gene: a putative integral membrane proteoglycan required for cell division patterning during postembryonic development of the nervous system in Drosophila1995 · 263 citations
  4. 4Stimulation of fibroblast growth factor receptor-1 occupancy and signaling by cell surface-associated syndecans and glypican.1996 · 274 citations
  5. 5Regulation of growth factor activation by proteoglycans: What is the role of the low affinity receptors?1995 · 475 citations