Novel NPHS1 Gene Mutation in an Iranian Patient with Congenital Nephrotic Syndrome of the Finnish Type

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Sonbol Amelia, Martin Zenkerb, Ameneh Zare-shahabadic, Seyed Taher Esfahania, Abbas Madania, Maryam Monajemzadeha, Behnaz Bazargania, Nematollah Ataeia, Niloofar Hajezadeha, Nima Rezaeid

a Tehran University of Medical Sciences, Pediatrics Center of Excellence, Children's Medical Center, Tehran, Iran,

b University Hospital of Magdeburg, Institute of Human Genetics, Magdeburg, Germany,

c Tehran University of Medical Sciences, Research Center for Immunodeficiencies, Children's Medical Center, Tehran, Iran,

d Tehran University of Medical Sciences, Research Center for Immunodeficiencies, Children's Medical Center; and Department of Immunology, School of Medicine, Tehran, Iran,

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ISSN: 02116995
Idioma original: Inglés

DOI:10.3265/Nefrologia.pre2013.Jun.11838

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2022 9	47	43	90
2022 8	40	52	92
2022 7	33	48	81
2022 6	43	55	98
2022 5	37	43	80
2022 4	45	42	87
2022 3	40	41	81
2022 2	46	56	102
2021 1	39	31	70
2021 12	55	53	108
2021 11	34	37	71
2021 10	42	41	83
2021 9	29	36	65
2021 8	43	43	86
2021 7	29	39	68
2021 6	28	24	52
2021 5	41	33	74
2021 4	99	90	189
2021 3	56	21	77
2021 2	63	18	81
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2020 6	34	17	51
2020 5	55	20	75
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2020 3	38	11	49
2020 2	37	24	61
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2019 3	26	21	47
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2018 5	78	20	98
2018 4	71	16	87
2018 3	82	16	98
2018 2	80	7	87
2018 1	88	13	101
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2017 11	54	6	60
2017 10	35	8	43
2017 9	52	13	65
2017 8	71	12	83
2017 7	67	11	78
2017 6	70	9	79
2017 5	75	12	87
2017 4	57	7	64
2017 3	49	6	55
2017 2	33	4	37
2016 1	23	3	26
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2016 5	145	0	145
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2016 3	101	0	101
2016 2	149	0	149
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2015 10	90	0	90
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