A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families. (Q51063406)

28 March 2018

title

A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families. (English)

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28 March 2018

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13

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Brian F Meyer

14

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author name string

Mohamed H Al-Hamed

1

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Essam Al-Sabban

2

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Hamad Al-Mojalli

3

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Naffaa Al-Harbi

4

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Eissa Faqeih

5

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Hammad Al Shaya

6

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Khalid Alhasan

7

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Safaa Al-Hissi

8

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Mohamed Rajab

9

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Noel Edwards

10

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Abbas Al-Abbad

11

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Ibrahim Al-Hassoun

12

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publication date

18 April 2013

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Journal of Human Genetics

published in

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volume

58

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page(s)

480-489

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issue

7

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https://scigraph.springernature.com/pub.10.1038/jhg.2013.27

exact match

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cites work

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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7 January 2021

The treatment of minimal change nephrotic syndrome (lipoid nephrosis): cooperative studies of the Arbeitsgemeinschaft für Pädiatrische Nephrologie (APN)

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7 January 2021

Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome

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7 January 2021

Focal segmental glomerulosclerosis in a patient homozygous for a CD2AP mutation

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7 January 2021

NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome

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7 January 2021

Identifiers

DOI

10.1038/JHG.2013.27

1 reference

28 March 2018

Dimensions Publication ID

0 references

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28 March 2018