Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). (Q34985759)

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30 January 2020

title

Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) (English)

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1

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Massimo Attanasio

3

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30 January 2020

Boris Utsch

9

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Sophie Saunier

14

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Corinne Antignac

15

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30 January 2020

author name string

K Tory

2

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W Zhou

4

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M Chaki

5

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Y Paruchuri

6

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30 January 2020

E L Wise

7

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M T F Wolf

8

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C Becker

10

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G Nürnberg

11

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P Nürnberg

12

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A Nayir

13

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F Hildebrandt

16

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language of work or name

English

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publication date

8 June 2009

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Journal of Medical Genetics

30 January 2020

published in

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volume

46

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page(s)

663-670

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issue

10

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