Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex | Journal of Medical Genetics

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Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex

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	Abstract	Full	Pdf
Nov 2021	1790	65	50
Dec 2021	315	254	56
Jan 2022	124	119	24
Feb 2022	113	110	29
Mar 2022	110	109	35
Apr 2022	117	117	24
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Aug 2022	194	187	38
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Dec 2022	239	236	35
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May 2023	85	75	43
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Oct 2023	91	86	35
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Dec 2023	141	127	20
Jan 2024	73	55	26
Feb 2024	60	57	17
Mar 2024	88	80	39
Total	5451	3488	1031