Wikidata

(Q34205653)

English

Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia

scientific article

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title
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017
author
Jan Senderek
object named as
Jan Senderek
series ordinal
3
0 references
author name string
Carsten Bergmann
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017
Klaus Zerres
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017
Sabine Rudnik-Schoneborn
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017
Thomas Eggermann
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017
Martin Häusler
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017
Michael Mull
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017
Vincent T Ramaekers
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017
page(s)
1537-1544
1 reference
stated in
Europe PubMed Central
PubMed ID
12805098
retrieved
31 July 2017

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