We have ascertained a large family with classical autosomal dominant
hereditary angioneurotic oedema. The affected members have been well characterised
at a clinical and immunological level.
Is anyone interested in receiving a DNA sample from an affected family
member for mutation studies in the C1NH gene?
Dr Graeme Suthers
MBBS, PhD, FRACP
SA Clinical Genetics Service
Centre for Medical Genetics
Women's & Children's Hospital
North Adelaide SA 5006
tel (08) 204 7375 (International prefix -61-8-)
fax (08) 204 6088 (International prefix -61-8-)