Report of a black South African child with oculodentodigital dysplasia and a novel GJA1 gene mutation

Liviu Feller; Neil H. Wood; Michelle D. Sluiter; Claudia Noffke; Erich J. Raubenheimer; Johan Lemmer; Elizabeth J. Van Rensburg

doi:10.1002/ajmg.a.32272

Report of a black South African child with oculodentodigital dysplasia and a novel GJA1 gene mutation

Liviu Feller^*
, Neil H. Wood
, Michelle D. Sluiter
, Claudia Noffke
, Erich J. Raubenheimer
, Johan Lemmer
, Elizabeth J. Van Rensburg

^*Corresponding author for this work

Periodontology and Oral Medicine

Research output: Contribution to journal › Letter › peer-review

15 Citations (Scopus)

Original language	English
Pages (from-to)	1350-1353
Number of pages	4
Journal	American Journal of Medical Genetics, Part A
Volume	146
Issue number	10
DOIs	https://doi.org/10.1002/ajmg.a.32272
Publication status	Published - 15 May 2008

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title = "Report of a black South African child with oculodentodigital dysplasia and a novel GJA1 gene mutation",

author = "Liviu Feller and Wood, \{Neil H.\} and Sluiter, \{Michelle D.\} and Claudia Noffke and Raubenheimer, \{Erich J.\} and Johan Lemmer and \{Van Rensburg\}, \{Elizabeth J.\}",

year = "2008",

month = may,

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doi = "10.1002/ajmg.a.32272",

language = "English",

volume = "146",

pages = "1350--1353",

journal = "American Journal of Medical Genetics, Part A",

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T1 - Report of a black South African child with oculodentodigital dysplasia and a novel GJA1 gene mutation

AU - Feller, Liviu

AU - Wood, Neil H.

AU - Sluiter, Michelle D.

AU - Noffke, Claudia

AU - Raubenheimer, Erich J.

AU - Lemmer, Johan

AU - Van Rensburg, Elizabeth J.

PY - 2008/5/15

Y1 - 2008/5/15

UR - https://www.scopus.com/pages/publications/43049137347

U2 - 10.1002/ajmg.a.32272

DO - 10.1002/ajmg.a.32272

M3 - Letter

C2 - 18412120

AN - SCOPUS:43049137347

SN - 1552-4825

VL - 146

SP - 1350

EP - 1353

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 10

ER -

Report of a black South African child with oculodentodigital dysplasia and a novel GJA1 gene mutation

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