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Garrison-Morton-Norman History of Medicine

BROWN, William Ted

1 entries in the GMN corpus.

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2003

#14217

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

COLLINS, Francis Sellers (1950 – )
COLLINS, Francis Sellers (1950 – ) ERIKSSON, Maria BROWN, William Ted GORDON, Leslie Beth & et al.

The authors showed that mutations in lamin A (LMNA) are the cause of Hutchinson-Gilford progeria sundrom (HGPS). At the end of their abstract they stated that "The discovery of the molecular basis of this disease may …