Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy
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Published:2021-02
Issue:2
Volume:23
Page:408-414
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
Parry David A., Martin Carol-Anne, Greene Philip, Marsh Joseph A., Ambrose J.C., Arumugam P., Baple E.L., Bleda M., Boardman-Pretty F., Boissiere J.M., Boustred C.R., Brittain H., Caulfield M.J., Chan G.C., Craig C.E.H., Daugherty L.C., de Burca A., Devereau A., Elgar G., Foulger R.E., Fowler T., Furió-Tarí P., Giess A., Hackett J.M., Halai D., Hamblin A., Henderson S., Holman J.E., Hubbard T.J.P., Ibáñez K., Jackson R., Jones L.J., Kasperaviciute D., Kayikci M., Kousathanas A., Lahnstein L., Lawson K., Leigh S.E.A., Leong I.U.S., Lopez F.J., Maleady-Crowe F., Mason J., McDonagh E.M., Moutsianas L., Mueller M., Murugaesu N., Need A.C., Odhams C.A., Orioli A., Patch C., Perez-Gil D., Pereira M.B., Polychronopoulos D., Pullinger J., Rahim T., Rendon A., Riesgo-Ferreiro P., Rogers T., Ryten M., Savage K., Sawant K., Scott R.H., Siddiq A., Sieghart A., Smedley D., Smith K.R., Smith S.C., Sosinsky A., Spooner W., Stevens H.E., Stuckey A., Sultana R., Tanguy M., Thomas E.R.A., Thompson S.R., Tregidgo C., Tucci A., Walsh E., Watters S.A., Welland M.J., Williams E., Witkowska K., Wood S.M., Zarowiecki M., Blyth Moira, Cox Helen, Donnelly Deirdre, Greenhalgh Lynn, Greville-Heygate Stephanie, Harrison Victoria, Lachlan Katherine, McKenna Caoimhe, Quigley Alan J., Rea Gillian, Robertson Lisa, Suri Mohnish, Jackson Andrew P.ORCID
Subject
Genetics (clinical)
Cited by
36 articles.
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