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Dofash, L.
6
results:
Search for persons
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Online (6)
Mediatypes
Articles (Online) (5)
OpenAccess-fulltext (1)
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1
P.01 A KLHL40 3′UTR splice-altering variant causes milder N..:
Dofash, L.
;
Monahan, G.
;
Servián-Morilla, E.
...
Neuromuscular Disorders. 32 (2022) - p. S45 , 2022
Link:
https://doi.org/10.1016/..
?
2
CONGENITAL MYOPATHIES – NEMALINE MYOPATHIES:
Dofash, L.
;
Faiz, F.
;
Servián-Morilla, E.
...
Neuromuscular Disorders. 31 (2021) - p. S60 , 2021
Link:
https://doi.org/10.1016/..
?
3
Three novel missense variants in two families with JAG2-ass..:
Dofash, Lein
;
Lyengar, Krishnan
;
Pereira, Nolette
...
Neuromuscular Disorders. , 2024
Link:
https://doi.org/10.1016/..
?
4
Ablation of the carboxy-terminal end of MAMDC2 causes a dis..:
Mavillard, Fabiola
;
Servian-Morilla, Emilia
;
Dofash, Lein
...
Brain. 146 (2023) 12 - p. 5235-5248 , 2023
Link:
https://doi.org/10.1093/..
?
5
AKLHL403' UTR splice-altering variant causes milder NEM8, a..:
Dofash, Lein N H
;
Monahan, Gavin V
;
Servián-Morilla, Emilia
...
Human Molecular Genetics. 32 (2022) 7 - p. 1127-1136 , 2022
Link:
https://doi.org/10.1093/..
?
6
A KLHL40 3' UTR splice-altering variant causes milder NEM8,..:
Dofash, Lein N. H
;
Monahan, Gavin V
;
Servián Morilla, E
...
Preprint. , 2022
Link:
http://hdl.handle.net/10..
1-6