000 02467 a2200805 4500
005 20250518101641.0
264 0 _c20200803
008 202008s 0 0 eng d
022 _a1546-1718
024 7 _a10.1038/s41588-020-0615-4
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCortese, Andrea
245 0 0 _aBiallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
_h[electronic resource]
260 _bNature genetics
_c05 2020
300 _a473-481 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
700 1 _aZhu, Yi
700 1 _aRebelo, Adriana P
700 1 _aNegri, Sara
700 1 _aCourel, Steve
700 1 _aAbreu, Lisa
700 1 _aBacon, Chelsea J
700 1 _aBai, Yunhong
700 1 _aBis-Brewer, Dana M
700 1 _aBugiardini, Enrico
700 1 _aBuglo, Elena
700 1 _aDanzi, Matt C
700 1 _aFeely, Shawna M E
700 1 _aAthanasiou-Fragkouli, Alkyoni
700 1 _aHaridy, Nourelhoda A
700 1 _aIsasi, Rosario
700 1 _aKhan, Alaa
700 1 _aLaurà, Matilde
700 1 _aMagri, Stefania
700 1 _aPipis, Menelaos
700 1 _aPisciotta, Chiara
700 1 _aPowell, Eric
700 1 _aRossor, Alexander M
700 1 _aSaveri, Paola
700 1 _aSowden, Janet E
700 1 _aTozza, Stefano
700 1 _aVandrovcova, Jana
700 1 _aDallman, Julia
700 1 _aGrignani, Elena
700 1 _aMarchioni, Enrico
700 1 _aScherer, Steven S
700 1 _aTang, Beisha
700 1 _aLin, Zhiqiang
700 1 _aAl-Ajmi, Abdullah
700 1 _aSchüle, Rebecca
700 1 _aSynofzik, Matthis
700 1 _aMaisonobe, Thierry
700 1 _aStojkovic, Tanya
700 1 _aAuer-Grumbach, Michaela
700 1 _aAbdelhamed, Mohamed A
700 1 _aHamed, Sherifa A
700 1 _aZhang, Ruxu
700 1 _aManganelli, Fiore
700 1 _aSantoro, Lucio
700 1 _aTaroni, Franco
700 1 _aPareyson, Davide
700 1 _aHoulden, Henry
700 1 _aHerrmann, David N
700 1 _aReilly, Mary M
700 1 _aShy, Michael E
700 1 _aZhai, R Grace
700 1 _aZuchner, Stephan
773 0 _tNature genetics
_gvol. 52
_gno. 5
_gp. 473-481
856 4 0 _uhttps://doi.org/10.1038/s41588-020-0615-4
_zAvailable from publisher's website
999 _c30932576
_d30932576