A known pathogenic variant in the essential mitochondrial translation gene RMND1 causes a Perrault‐like syndrome with renal defects
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Published in | Clinical genetics Vol. 94; no. 2; pp. 276 - 277 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.08.2018
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Subjects | |
Online Access | Get full text |
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Bibliography: | SourceType-Other Sources-1 ObjectType-Article-2 content type line 63 ObjectType-Correspondence-1 |
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ISSN: | 0009-9163 1399-0004 |
DOI: | 10.1111/cge.13255 |