A Novel Synergistic Association of Variants in PTRH2 and KIF1A Relates to a Syndrome of Hereditary Axonopathy, Outer Hair Cell Dysfunction, Intellectual Disability, Pancreatic Lipomatosis, Diabetes, Cerebellar Atrophy, and Vertebral Artery Hypoplasia
2018 ◽
Vol 2018.29
(0)
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pp. 2B11
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2015 ◽
Vol 17
(2)
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pp. 89-101
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Keyword(s):
2012 ◽
Vol 13
(4)
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pp. 485-504
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Keyword(s):