Recessive mutations in COL25A1 are a cause of congenital cranial dysinnervation disorder (Q34902957)

5 August 2017

title

Recessive mutations in COL25A1 are a cause of congenital cranial dysinnervation disorder (English)

1 reference

5 August 2017

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Nada Al Tassan

9

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author name string

Jameela M A Shinwari

1

1 reference

5 August 2017

Arif Khan

2

1 reference

5 August 2017

Salma Awad

3

1 reference

5 August 2017

Zakia Shinwari

4

1 reference

5 August 2017

Ayodele Alaiya

5

1 reference

5 August 2017

Mohamad Alanazi

6

1 reference

5 August 2017

Asma Tahir

7

1 reference

5 August 2017

Coralie Poizat

8

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5 August 2017

language of work or name

English

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publication date

11 December 2014

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American Journal of Human Genetics

5 August 2017

published in

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5 August 2017

volume

96

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5 August 2017

issue

1

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5 August 2017

page(s)

147-152

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Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2.

5 August 2017

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2

8 July 2018

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8 July 2018

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8 July 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/25500261

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25500261

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2014.11.006

1 reference

5 August 2017

1 reference

5 August 2017

1 reference