PMID- 33766980
OWN - NLM
STAT- MEDLINE
DCOM- 20210514
LR  - 20231031
IS  - 1757-790X (Electronic)
IS  - 1757-790X (Linking)
VI  - 14
IP  - 3
DP  - 2021 Mar 25
TI  - Typical MRI features of PLA2G6 mutation-related phospholipase-associated 
      neurodegeneration (PLAN)/infantile neuroaxonal dystrophy (INAD).
LID - 10.1136/bcr-2021-242586 [doi]
LID - e242586
FAU - Singh, Somesh
AU  - Singh S
AD  - Radiodiagnosis, SGPGIMS, Lucknow, Uttar Pradesh, India.
FAU - Mishra, Sarvesh Chandra
AU  - Mishra SC
AD  - Radiodiagnosis, SGPGIMS, Lucknow, Uttar Pradesh, India.
FAU - Israrahmed, Amrin
AU  - Israrahmed A
AD  - Radiodiagnosis, SGPGIMS, Lucknow, Uttar Pradesh, India.
FAU - Lal, Hira
AU  - Lal H
AD  - Radiodiagnosis, Sanjay Gandhi Post Graduate Institute of Medical Sciences, 
      Lucknow, India hiralal2007@yahoo.co.in.
LA  - eng
PT  - Case Reports
PT  - Journal Article
DEP - 20210325
PL  - England
TA  - BMJ Case Rep
JT  - BMJ case reports
JID - 101526291
RN  - EC 3.1.- (Phospholipases)
RN  - EC 3.1.1.4 (Group VI Phospholipases A2)
RN  - EC 3.1.1.4 (PLA2G6 protein, human)
SB  - IM
MH  - Group VI Phospholipases A2/genetics
MH  - Humans
MH  - Magnetic Resonance Imaging
MH  - Mutation
MH  - *Neuroaxonal Dystrophies/diagnostic imaging/genetics
MH  - *Phospholipases
PMC - PMC8006834
OTO - NOTNLM
OT  - developmental paediatrocs
OT  - genetics
OT  - radiology
COIS- Competing interests: None declared.
EDAT- 2021/03/27 06:00
MHDA- 2021/05/15 06:00
PMCR- 2023/03/25
CRDT- 2021/03/26 06:15
PHST- 2021/03/26 06:15 [entrez]
PHST- 2021/03/27 06:00 [pubmed]
PHST- 2021/05/15 06:00 [medline]
PHST- 2023/03/25 00:00 [pmc-release]
AID - 14/3/e242586 [pii]
AID - bcr-2021-242586 [pii]
AID - 10.1136/bcr-2021-242586 [doi]
PST - epublish
SO  - BMJ Case Rep. 2021 Mar 25;14(3):e242586. doi: 10.1136/bcr-2021-242586.