Single amino acid variation in MAB21L1 is dominantly associated with congenital eye defects | Journal of Medical Genetics

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Original research

Single amino acid variation in MAB21L1 is dominantly associated with congenital eye defects

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Online download statistics by month: November 2022 to August 2024

	Abstract	Full	Pdf
Nov 2022	175	9	11
Dec 2022	482	44	33
Jan 2023	513	14	4
Feb 2023	188	8	1
Mar 2023	205	12	15
Apr 2023	166	14	8
May 2023	123	4	1
Jun 2023	444	23	10
Jul 2023	348	37	20
Aug 2023	289	11	5
Sep 2023	74	5	4
Oct 2023	68	7	4
Nov 2023	92	7	6
Dec 2023	63	9	8
Jan 2024	169	9	0
Feb 2024	57	11	2
Mar 2024	99	8	3
Apr 2024	86	4	0
May 2024	168	2	2
Jun 2024	77	3	1
Jul 2024	70	2	2
Aug 2024	85	6	3
Total	4041	249	143