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Published in 2018 at "Clinical Genetics"
DOI: 10.1111/cge.13361
Abstract: Our patient represents the third case of pheochromocytoma and mental retardation involving a homozygous region in 2p11.2 with a TMEM127 variant. This rare homozygous mutation does not seem to aggravate the clinical picture of the…
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Keywords:
new case;
pheochromocytomas involving;
bilateral pheochromocytomas;
case ... See more keywords