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- Fri Feb 24, 2017 1:02 am
- Forum: Genetics
- Topic: Congenital disorders of glycosylation
- Replies: 0
- Views: 3447
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...