Congenital disorders of glycosylation

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      zcbtwfi
      Participant

      Hello all,

      Can someone please explain to me whether (and why) the autosomal recessive congenital disorders of glycosylation (specifically Type 1a PMM) are an example of Pleiotropy, Complementation, Gene Interaction, Translocation, Epistasis, Incomplete penetrance or Multiple alleles as I am a little unsure as to the concept this condition is based upon.

      Many thanks,

      Rita

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