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Novel STAMBP mutation and additional findings in an Arabic family |
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| Authors: | Eissa A. Faqeih Laila Bastaki Rasim Ozgur Rosti Emily G. Spencer AbdulAli P. Zada Mohammad A. M. Saleh Kyongmi Um Joseph G. Gleeson |
| Affiliation: | 1. Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia;2. Kuwait Medical Genetics Centre, Maternity Hospital, Safat, Kuwait;3. Department of Neurosciences and Pediatrics, Howard Hughes Medical Institute, University of California, San Diego, California;4. Department of Pathology and Clinical Laboratory Medicine, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia |
| Abstract: | |
| Keywords: | MIC‐CAP syndrome STAMBP gene capillary malformation congenital hypothyroidism alopecia areata |