New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes-Reference-Cited by-同舟云学术

New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes

Published:2006-12 Issue:12 Volume:21 Page:2237-2240
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Devos David,Vuillaume Isabelle,De Becdelievre Alix,De Martinville Berengère,Dhaenens Claire-Marie,Cuvellier Jean-Christophe,Cuisset Jean-Marie,Vallée Louis,Lemaitre Marie-Pierre,Bourteel Hélène,Hachulla Eric,Wallaert Benoit,Destée Alain,Defebvre Luc,Sablonnière Bernard

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference15 articles.

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4. Brain-thyroid-lung syndrome: a patient with a severe multi-system disorder due to a de novo mutation in the thyroid transcription factor 1 gene;Willemsen;Eur J Pediatr,2005

5. Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure;Iwatani;J Pediatr,2000

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