SLC26A2disease spectrum in Sweden - high frequency of recessive multiple epiphyseal dysplasia (rMED)-Reference-Cited by-同舟云学术

SLC26A2disease spectrum in Sweden - high frequency of recessive multiple epiphyseal dysplasia (rMED)

Author:

Mäkitie O.¹²³,Geiberger S.⁴,Horemuzova E.⁵⁶,Hagenäs L.⁵⁶,Moström E.⁷,Nordenskjöld M.¹²,Grigelioniene G.¹²,Nordgren A.¹²

Affiliation:

1. Department of Molecular Medicine and Surgery; Karolinska Institutet; Stockholm Sweden

2. Department of Clinical Genetics; Karolinska University Hospital; Stockholm Sweden

3. Folkhälsan Institute of Genetics; Helsinki Finland

4. Department of Pediatric Radiology; Karolinska University Hospital Solna; Stockholm Sweden

5. Department for Women's and Children's Health; Karolinska Institutet; Stockholm Sweden

6. Pediatric Endocrinology Unit; Karolinska University Hospital; Stockholm Sweden

7. Department of Pediatric Orthopaedic Surgery; Karolinska University Hospital; Stockholm Sweden

Funder

Academy of Finland

Folkhï¿½lsan Research Foundation

Sigrid Juselius Foundation

Swedish Research Council

The Swedish Childhood Cancer Foundation

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

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