Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 gene | BMJ Case Reports

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Case report

Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 gene

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	Abstract	Full	Pdf
Oct 2021	981	13	4
Nov 2021	832	6	5
Dec 2021	310	2	4
Jan 2022	209	11	2
Feb 2022	87	5	4
Mar 2022	97	4	4
Apr 2022	60	0	0
May 2022	83	3	1
Jun 2022	116	8	0
Jul 2022	56	3	2
Aug 2022	75	5	2
Sep 2022	79	3	0
Oct 2022	64	1	0
Nov 2022	98	2	0
Dec 2022	44	2	1
Jan 2023	161	1	2
Feb 2023	66	3	1
Mar 2023	103	3	4
Apr 2023	26	0	1
May 2023	14	6	0
Jun 2023	42	1	0
Jul 2023	40	0	0
Aug 2023	32	1	0
Sep 2023	38	2	0
Oct 2023	40	0	0
Nov 2023	20	1	0
Dec 2023	40	2	3
Jan 2024	32	1	0
Feb 2024	37	1	1
Mar 2024	41	1	0
Apr 2024	28	0	0
Total	3951	91	41