Dr Geoffrey Pollitt

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منابع مشابه

Pollitt syndrome patients carry mutation in TTDN1

Complete human genome sequencing was used to identify the causative mutation in a family with Pollitt syndrome (MIM #275550), comprising two non-consanguineous parents and their two affected children. The patient's symptoms were reminiscent of the non-photosensitive form of recessively inherited trichothiodystrophy (TTD). A mutation in the TTDN1/C7orf11 gene, a gene that is known to be involved...

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ژورنال

عنوان ژورنال: The Psychiatrist

سال: 2010

ISSN: 1758-3209,1758-3217

DOI: 10.1192/pb.bp.109.029033