| 000 | 01176 a2200325 4500 | ||
|---|---|---|---|
| 005 | 20250517152725.0 | ||
| 008 | ####s 0 0 eng d | ||
| 022 | _a1460-2083 | ||
| 024 | 7 |
_a10.1093/hmg/ddx130 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aRouzier, Cécile | |
| 245 | 0 | 0 |
_aA novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions. _h[electronic resource] |
| 260 |
_bHuman molecular genetics _c05 2017 |
||
| 300 |
_a1786 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Published Erratum | ||
| 700 | 1 | _aMoore, David | |
| 700 | 1 | _aDelorme, Cécile | |
| 700 | 1 | _aLacas-Gervais, Sandra | |
| 700 | 1 | _aAit-El-Mkadem, Samira | |
| 700 | 1 | _aFragaki, Konstantina | |
| 700 | 1 | _aBurté, Florence | |
| 700 | 1 | _aSerre, Valérie | |
| 700 | 1 | _aBannwarth, Sylvie | |
| 700 | 1 | _aChaussenot, Annabelle | |
| 700 | 1 | _aCatala, Martin | |
| 700 | 1 | _aYu-Wai-Man, Patrick | |
| 700 | 1 | _aPaquis-Flucklinger, Véronique | |
| 773 | 0 |
_tHuman molecular genetics _gvol. 26 _gno. 9 _gp. 1786 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1093/hmg/ddx130 _zAvailable from publisher's website |
| 999 |
_c27145457 _d27145457 |
||