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Details for article 1 of 11 found articles
| Title: |
A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency |
| Author: |
Alston, Charlotte L. Ceccatelli Berti, Camilla Blakely, Emma L. Oláhová, Monika He, Langping McMahon, Colin J. Olpin, Simon E. Hargreaves, Iain P. Nolli, Cecilia McFarland, Robert Goffrini, Paola O’Sullivan, Maureen J. Taylor, Robert W. |
| Appeared in: |
Human genetics |
| Paging: | Volume 134 (2015) nr. 8 pages 869-879 |
| Year: |
2015 |
| Contents: | |
| Publisher: |
Springer Berlin Heidelberg, Berlin/Heidelberg |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 1 of 11 found articles
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