Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association.

Authors	M Mancuso, M C Bianchi, F M Santorelli, A Tessa, C Casali, L Murri, G Siciliano
Journal	Journal of neurology (J Neurol) Vol. 246 Issue 12 Pg. 1197-8 (Dec 1999) ISSN: 0340-5354 [Print] Germany
PMID	10653316 (Publication Type: Case Reports, Letter)
Chemical References	DNA, Mitochondrial
Topics	DNA, Mitochondrial (genetics) Gene Deletion Humans Lipomatosis (complications) Male Middle Aged Mitochondrial Encephalomyopathies (complications, genetics) Pedigree

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!