Connecting you to content on EBSCOhost

Works by Croxen, R

Results: 4

1

Correction: Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.

Published in:

Nature Genetics, 2001, v. 29, n. 1, p. 100, doi. 10.1038/ng0901-100b

By:

Spelbrink, J.N.;
Li, F.-Y.;
Tiranti, V.;
Nikali, K.;
Yuan, Q.-P.;
Tariq, M.;
Wanrooij, S.;
Garrido, N.;
Comi, G.;
Morandi, L.;
Santoro, L.;
Toscano, A.;
Fabrizi, G.-M.;
Somer, H.;
Croxen, R.;
Beeson, D.;
Poultron, J.;
Suomalainen, A.;
Jacobs, H.T.

Publication type:

Article

2

End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations.

Published in:

2001

By:

Croxen, R;
Young, C;
Slater, C;
Haslam, S;
Brydson, M;
Vincent, A;
Beeson, D

Publication type:

journal article

3

Novel functional epsilon-subunit polypeptide generated by a single nucleotide deletion in acetylcholine receptor deficiency congenital myasthenic syndrome.

Published in:

1999

By:

Croxen, R;
Newland, C;
Betty, M;
Vincent, A;
Newsom-Davis, J;
Beeson, D

Publication type:

journal article

4

Congenital Myasthenic Syndromes: Studies of the AChR and Other Candidate Genes<sup>a</sup>.

Published in:

Annals of the New York Academy of Sciences, 1998, v. 841, n. 1, p. 181, doi. 10.1111/j.1749-6632.1998.tb10924.x

By:

BEESON, D.;
NEWLAND, C.;
CROXEN, R.;
BUCKEL, A.;
LI, F-Y.;
LARSSON, C.;
TARIQ, M.;
VINCENT, A.;
NEWSOM-DAVIS, J.

Publication type:

Article