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Homozygous loss of function

Crosby AH (2004) Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase. Nat Genet 36 1225-1229... [Pg.1690]

See other pages where Homozygous loss of function is mentioned: [Pg.748]    [Pg.465]   
See also in sourсe #XX -- [ Pg.82 , Pg.83 ]

See also in sourсe #XX -- [ Pg.82 , Pg.83 ]



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