Correction to: The evolution of the mitochondrial disease diagnostic odyssey
| Medienart: |
E-Artikel |
|---|
| Erscheinungsjahr: |
2023 |
|---|---|
| Erschienen: |
2023 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:18 |
|---|---|
| Enthalten in: |
Orphanet journal of rare diseases - 18(2023), 1 vom: 20. Juli |
| Sprache: |
Englisch |
|---|
| Beteiligte Personen: |
Thompson, John L. P. [VerfasserIn] |
|---|
| Links: |
Volltext [kostenfrei] |
|---|
| Anmerkungen: |
© The Author(s) 2023 |
|---|
| doi: |
10.1186/s13023-023-02832-0 |
|---|
| funding: |
|
|---|---|
| Förderinstitution / Projekttitel: |
|
| PPN (Katalog-ID): |
SPR052323307 |
|---|
| LEADER | 01000naa a22002652 4500 | ||
|---|---|---|---|
| 001 | SPR052323307 | ||
| 003 | DE-627 | ||
| 005 | 20230721064738.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 230721s2023 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1186/s13023-023-02832-0 |2 doi | |
| 035 | |a (DE-627)SPR052323307 | ||
| 035 | |a (SPR)s13023-023-02832-0-e | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 100 | 1 | |a Thompson, John L. P. |e verfasserin |0 (orcid)0000-0002-5089-0967 |4 aut | |
| 245 | 1 | 0 | |a Correction to: The evolution of the mitochondrial disease diagnostic odyssey |
| 264 | 1 | |c 2023 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a Computermedien |b c |2 rdamedia | ||
| 338 | |a Online-Ressource |b cr |2 rdacarrier | ||
| 500 | |a © The Author(s) 2023 | ||
| 700 | 1 | |a Karaa, Amel |4 aut | |
| 700 | 1 | |a Pham, Hung |4 aut | |
| 700 | 1 | |a Yeske, Philip |4 aut | |
| 700 | 1 | |a Krischer, Jeffrey |4 aut | |
| 700 | 1 | |a Xiao, Yi |4 aut | |
| 700 | 1 | |a Long, Yuelin |4 aut | |
| 700 | 1 | |a Kramer, Amanda |4 aut | |
| 700 | 1 | |a Dimmock, David |4 aut | |
| 700 | 1 | |a Holbert, Amy |4 aut | |
| 700 | 1 | |a Gorski, Cliff |4 aut | |
| 700 | 1 | |a Engelstad, Kristin M. |4 aut | |
| 700 | 1 | |a Buchsbaum, Richard |4 aut | |
| 700 | 1 | |a Rosales, Xiomara Q. |4 aut | |
| 700 | 1 | |a Hirano, Michio |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Orphanet journal of rare diseases |d London : BioMed Central, 2006 |g 18(2023), 1 vom: 20. Juli |w (DE-627)SPR029480884 |w (DE-600)2225857-7 |x 1750-1172 |7 nnns |
| 773 | 1 | 8 | |g volume:18 |g year:2023 |g number:1 |g day:20 |g month:07 |
| 856 | 4 | 0 | |u https://dx.doi.org/10.1186/s13023-023-02832-0 |z kostenfrei |3 Volltext |
| 912 | |a GBV_USEFLAG_A | ||
| 912 | |a GBV_SPRINGER | ||
| 951 | |a AR | ||
| 952 | |d 18 |j 2023 |e 1 |b 20 |c 07 | ||