The human holocytochrome c-type synthetase (HCCS) gene is located on Xp22.3 and is one of the genes identified in a 450-Kb region deleted in the neurodevelopmental disorder microphthalmia with linear skin defects. Several other developmental disorders with or without a neurological phenotype have be
β¦ LIBER β¦
Refinement of the genomic structure ofSTX1A and mutation analysis in nondeletion Williams syndrome patients
β Scribed by Wu, Yuan-Qing ;Bejjani, Bassem A. ;Tsui, Lap-Chee ;Mandel, Ariane ;Osborne, Lucy R. ;Shaffer, Lisa G.
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 95 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0148-7299
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