Erratum to Identification of Novel Mutations Confirms PDE4D as a Major Gene Causing Acrodysostosis [Human Mutation, 34, 1 (97-102)] DOI 10.1002/humu.22222];Identification of Novel Mutations Confirms Pde4d as a Major Gene Causing Acrodysostosis

Human Mutation

Volumn 34, Issue 1, 2013, Pages 97-102

  Lynch, Danielle C ^a   Dyment, David A ^b   Huang, Lijia ^b   Nikkel, Sarah M ^b   Lacombe, Didier ^c,d   Campeau, Philippe M ^e   Lee, Brendan ^e,f   Bacino, Carlos A ^e,g   Michaud, Jacques L ^h   Bernier, Francois P ^a   Parboosingh, Jillian S ^a   Innes, A Micheil ^a  

^a UNIVERSITY OF CALGARY   (Canada)

^b CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^c BORDEAUX UNIVERSITY HOSPITAL   (France)

^d UNIVERSITÉ DE BORDEAUX   (France)

^e BAYLOR COLLEGE OF MEDICINE   (United States)

^f HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^g Texas Children's Hospital   (United States)

^h UNIVERSITY OF MONTREAL   (Canada)

Author keywords

Acrodysostosis; Brachydactyly; Mutations; Obesity; Pde4d

Indexed keywords

CYCLIC AMP;

ACRODYSOSTOSIS; ADULT; ARTICLE; BRACHYDACTYLY; CHILD; CLINICAL ARTICLE; COGNITIVE DEFECT; DYSOSTOSIS; ENDOCRINE DISEASE; FEMALE; GENE; GENE MUTATION; HUMAN; LIPOLYSIS; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; MISSENSE MUTATION; OBESITY; PHOSPHODIESTERASE GENE; PRESCHOOL CHILD; PRIORITY JOURNAL; PSEUDOHYPOPARATHYROIDISM; PSEUDOPSEUDOHYPOPARATHYROIDISM; SCHOOL CHILD; SHORT STATURE;

EID: 84871610632     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22290     Document Type: Erratum

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