(Q54442301)

29 May 2018

title

Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral ectopia lentis. (English)

1 reference

29 May 2018

1 reference

0 references

V Bennouna Greene

1

1 reference

29 May 2018

C Stoetzel

2

1 reference

29 May 2018

V Pelletier

3

1 reference

29 May 2018

Y Perdomo-Trujillo

4

1 reference

29 May 2018

L Liebermann

5

1 reference

29 May 2018

V Marion

6

1 reference

29 May 2018

H De Korvin

7

1 reference

29 May 2018

C Boileau

8

1 reference

29 May 2018

J L Dufier

9

1 reference

29 May 2018

H Dollfus

10

1 reference

29 May 2018

publication date

1 March 2010

1 reference

29 May 2018

published in

Ophthalmic Genetics

1 reference

29 May 2018

volume

31

1 reference

29 May 2018

issue

1

1 reference

29 May 2018

page(s)

47-51

1 reference

29 May 2018

A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis

cites work

1 reference

https://api.crossref.org/works/10.3109%2F13816810903567604

Null mutations in LTBP2 cause primary congenital glaucoma

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810903567604

A disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motifs: the ADAMTS family

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810903567604

Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810903567604

ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810903567604

ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810903567604

TSRC1, a widely expressed gene containing seven thrombospondin type I repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810903567604

Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810903567604

10.3109/13816810903567604

21 January 2018

Identifiers

DOI

1 reference

29 May 2018

1 reference

29 May 2018