Taxon:

Human

Gene:

amyloid beta A4 precursor protein, APP

Chromosome:

21

Location:

21q21

Description:

Hereditary cerebral haemorrhage with amyloidosis-Dutch type has a higher mortality rate when paternally transmitted (Bornebroek M et al, 1997). HCHWA-D is an autosomal dominant disorder caused by a single base change in the amyloid beta A4 precursor protein gene on chromosome 21.

Category:

Parental effect

Record:

133

Last Modified 4/30/2010

Links:

OMIM  


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