(Q83021110)

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An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis

scientific article published on 01 June 2006

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16575393%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16575393%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

author name string

Abraham Zlotogorski

1

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18 January 2020

Dina Marek

2

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18 January 2020

Liran Horev

3

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18 January 2020

Almogit Abu

4

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18 January 2020

Dan Ben-Amitai

5

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18 January 2020

Liora Gerad

6

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18 January 2020

Arieh Ingber

7

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18 January 2020

Moshe Frydman

8

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18 January 2020

Haike Reznik-Wolf

9

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18 January 2020

Daniel A Vardy

10

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18 January 2020

Elon Pras

11

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18 January 2020

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1 June 2006

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18 January 2020

Journal of Investigative Dermatology

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18 January 2020

126

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18 January 2020

6

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18 January 2020

1292-1296

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18 January 2020

https://scigraph.springernature.com/pub.10.1038/sj.jid.5700251

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