Congenital disorders of glycosylation

Genetics as it applies to evolution, molecular biology, and medical aspects.

Moderators: honeev, Leonid, amiradm, BioTeam

Post Reply
zcbtwfi
Garter
Garter
Posts: 1
Joined: Fri Feb 24, 2017 12:57 am

Congenital disorders of glycosylation

Post by zcbtwfi » Fri Feb 24, 2017 1:02 am

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

Post Reply

Who is online

Users browsing this forum: No registered users and 8 guests