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Bi-allelic variants in the mitochondrial RNase P subunit PR..:

Hochberg, Irit ; Demain, Leigh A. M ; Richer, Julie...
Reproducció del document publicat a: https://doi.org/10.1016/j.ajhg.2021.10.002. , 2021

Link: http://hdl.handle.net/2445/181732

RT Journal
T1 <Title>Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftubarcepubl:oai:diposit.ub.edu:2445_181732&Exemplar=1&LAN=DE
				
A1 Hochberg, Irit
A1 Demain, Leigh A. M
A1 Richer, Julie
A1 Thompson, Kyle
A1 Urquhart, Jill E
A1 Rea, Alessandro
A1 Pagarkar, Waheeda
A1 Rodríguez Palmero, Agustí
A1 Schlüter, Agatha
A1 Verdura, Edgard
A1 Pujol, Aurora
A1 Quijada Fraile, Pilar
A1 Amberger, Albert
A1 Deutschmann, Andrea J
A1 Demetz, Sandra
A1 Gillespie, Meredith
A1 Belyantseva, Inna A
A1 Mcmillan, Hugh J
A1 Barzik, Melanie
A1 Beaman, Glenda M
A1 Motha, Reeya
A1 Ng, Kah Ying
A1 O'sullivan, James
A1 Williams, Simon G
A1 Bhaskar, Sanjeev S
A1 Lawrence, Isabella R
A1 Jenkinson, Emma M
A1 Zambonin, Jessica L
A1 Blumenfeld, Zeev
A1 Yalonetsky, Sergey
A1 Oerum, Stephanie
A1 Rossmanith, Walter
A1 Yue, Wyatt W
A1 Zschocke, Johannes
A1 Munro, Kevin J
A1 Battersby, Brendan J
A1 Friedman, Thomas B
A1 Taylor, Robert W
A1 O'keefe, Raymond T
A1 Newman, William G
PB Elsevier BV
YR 2021
K1 Malalties de l'ovari
K1 Malalties rares
K1 Ovary diseases
K1 Rare diseases
JF Reproducció del document publicat a: https://doi.org/10.1016/j.ajhg.2021.10.002
LK http://hdl.handle.net/2445/181732
DO http://hdl.handle.net/2445/181732
SF ELIB - SuUB Bremen

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