Allan–Herndon–Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH-Reference-Cited by-同舟云学术

Allan–Herndon–Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH

Published:2010-11 Issue:6 Volume:53 Page:392-395
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Boccone Loredana,Mariotti Stefano,Dessì Valentina,Pruna Dario,Meloni Antonella,Loudianos Georgios

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference26 articles.

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