Single large-scale mitochondrial DNA deletion syndromes: scientific and family conference optimizes the collection of rare disease research outcomes
Abstract Background The SLSMDS Research Network is a collaborative network comprising patient advocates, researchers, clinicians, and affected families seeking to improve outcomes for individuals with single large-scale mitochondrial DNA deletion syndromes (SLSMDS). Building off of jointly developed...
Saved in:
| Main Authors: | Laura E. MacMullen, Elizabeth Reynolds, Marissa Weis, Ibrahim George-Sankoh, Sara Nguyen, Katelynn D. Stanley, Mariya Redko, Maria Poblete, Amy C. Goldstein, Rebecca D. Ganetzky |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2025-08-01
|
| Series: | Orphanet Journal of Rare Diseases |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s13023-025-03632-4 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Severe clinical manifestation of mitochondrial disease due to the m.3243A>T variant: a case report of early-onset, multi-organ involvement and premature death
by: Hannah Gillespie, et al.
Published: (2025-08-01) -
Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability
by: Direnis Erdinc, et al.
Published: (2023-04-01) -
A Novel 3670-Base Pair Mitochondrial DNA Deletion Resulting in Multi-systemic Manifestations in a Child
by: Hsin-Ming Liu, et al.
Published: (2012-08-01) -
FAMILIAL CASE OF CHROMOSOME 22q11.2 DELETION SYNDROME
by: I. A. Tuzankina, et al.
Published: (2017-01-01) -
An in-frame deletion mutation in MLH1 drives Lynch syndrome-associated colorectal cancer
by: Xiaojuan Lin, et al.
Published: (2025-07-01)