Function of Tuberin and Hamartin in Tuberous Sclerosis Pathogenesis

J Gordon Millichap

doi:10.15844/pedneurbriefs-18-1-7

Function of Tuberin and Hamartin in Tuberous Sclerosis Pathogenesis

Pediatric Neurology Briefs

Volume 18 (2004): Issue 1

By: J Gordon Millichap

Open Access

|Jan 2004

Abstract

The genetics and function of tuberin and hamartin in the pathogenesis of tuberous sclerosis complex (TS) are reviewed in a presentation at a “Festschrift” honoring Dr Michael J Painter of the Division of Pediatric Neurology, Children’s Hospital of Pittsburgh, PA.

References

Narayanan V Tuberous sclerosis complex: genetics to pathogenesis Pediatr Neurol 2003 Nov 29 5 404 409 10.1016/j.pediatrneurol.2003.09.002 14684235
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Charrow J Progress in Pediatric Neurology III 1997 PNB Publ 435 439 Chpt 10
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-18-1-7 | Journal eISSN: 2166-6482

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Language: English

Page range: 6 - 6

Published on: Jan 1, 2004

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Tuberin and Hamartin,

Tuberous Sclerosis Complex,

Festschrift

© 2004 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 18 (2004): Issue 1