The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes (vol 52, pg 147, 2015)

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作者：
Waters, A. M.
Asfahani, R.
Carroll, P.
Bicknell, L.
Lescai, F.
Bright, A.
Chanudet, E.
Brooks, A.
Christou-Savina, S.
Osman, G.
Walsh, P.
Bacchelli, C.
Chagpier, A.
Vernay, B.
Bader, D. M.
Deshpande, C.
O'Sullivan, M.
Ocaka, L.
Stanescu, H.
Stewart, H. S.
Hildebrandt, F.
Otto, E.
Johnson, C. A.
Szymanska, K.
Katsanis, N.
Davis, E.
Kleta, R.
Hubank, M.
Doxsey, S.
Jackson, A.
Stupka, E.
Winey, M.
Beales, P. L.
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JOURNAL OF MEDICAL GENETICS | 2016年 / 53卷 / 12期
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中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
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页码：845 / 845
页数：1
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[1]   The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes [J].
Waters, Aoife M. ;
Asfahani, Rowan ;
Carroll, Paula ;
Bicknell, Louise ;
Lescai, Francesco ;
Bright, Alison ;
Chanudet, Estelle ;
Brooks, Anthony ;
Christou-Savina, Sonja ;
Osman, Guled ;
Walsh, Patrick ;
Bacchelli, Chiara ;
Chapgier, Ariane ;
Vernay, Bertrand ;
Bader, David M. ;
Deshpande, Charu ;
O' Sullivan, Mary ;
Ocaka, Louise ;
Stanescu, Horia ;
Stewart, Helen S. ;
Hildebrandt, Friedhelm ;
Otto, Edgar ;
Johnson, Colin A. ;
Szymanska, Katarzyna ;
Katsanis, Nicholas ;
Davis, Erica ;
Kleta, Robert ;
Hubank, Mike ;
Doxsey, Stephen ;
Jackson, Andrew ;
Stupka, Elia ;
Winey, Mark ;
Beales, Philip L. .
JOURNAL OF MEDICAL GENETICS, 2015, 52 (03) :147-156
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