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@article{Schon:2021:10.1136/bmj-2021-066288,
author = {Schon, KR and Horvath, R and Wei, W and Calabrese, C and Tucci, A and Ibanez, K and Ratnaike, T and Pitceathly, RDS and Bugiardini, E and Quinlivan, R and Hanna, MG and Clement, E and Ashton, E and Sayer, JA and Brennan, P and Josifova, D and Izatt, L and Fratter, C and Nesbitt, V and Barrett, T and McMullen, DJ and Smith, A and Deshpande, C and Smithson, SF and Festenstein, R and Canham, N and Caulfield, M and Houlden, H and Rahman, S and Chinnery, PF},
doi = {10.1136/bmj-2021-066288},
journal = {BMJ-BRITISH MEDICAL JOURNAL},
title = {Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study},
url = {http://dx.doi.org/10.1136/bmj-2021-066288},
volume = {375},
year = {2021}
}

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TY  - JOUR
AU  - Schon,KR
AU  - Horvath,R
AU  - Wei,W
AU  - Calabrese,C
AU  - Tucci,A
AU  - Ibanez,K
AU  - Ratnaike,T
AU  - Pitceathly,RDS
AU  - Bugiardini,E
AU  - Quinlivan,R
AU  - Hanna,MG
AU  - Clement,E
AU  - Ashton,E
AU  - Sayer,JA
AU  - Brennan,P
AU  - Josifova,D
AU  - Izatt,L
AU  - Fratter,C
AU  - Nesbitt,V
AU  - Barrett,T
AU  - McMullen,DJ
AU  - Smith,A
AU  - Deshpande,C
AU  - Smithson,SF
AU  - Festenstein,R
AU  - Canham,N
AU  - Caulfield,M
AU  - Houlden,H
AU  - Rahman,S
AU  - Chinnery,PF
DO  - 10.1136/bmj-2021-066288
PY  - 2021///
SN  - 0959-535X
TI  - Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study
T2  - BMJ-BRITISH MEDICAL JOURNAL
UR  - http://dx.doi.org/10.1136/bmj-2021-066288
UR  - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000718886700012&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
VL  - 375
ER  -

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