(Q28290728)

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Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

scientific article published on August 1, 1995

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title

Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3 (English)

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main subject

brain

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X-linked nonsyndromic deafness

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1 reference

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Silvère M van der Maarel

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6

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S. M. van der Maarel

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Europe PubMed Central

PubMed publication ID

7581392

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7581392

retrieved

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author name string

M. Bitner-Glindzicz

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1

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7581392

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22 May 2024

P. Turnpenny

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2

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Europe PubMed Central

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7581392

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7581392

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22 May 2024

P. Höglund

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3

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7581392

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H. Kääriäinen

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4

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7581392

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22 May 2024

E. M. Sankila

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5

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7581392

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22 May 2024

Y. J. de Kok

series ordinal

7

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PubMed publication ID

7581392

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7581392

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22 May 2024

H. H. Ropers

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8

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7581392

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F. P. Cremers

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9

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7581392

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22 May 2024

M. Pembrey

series ordinal

10

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Europe PubMed Central

PubMed publication ID

7581392

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7581392

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language of work or name

English

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publication date

August 1995

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published in

Human Molecular Genetics

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volume

4

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issue

8

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page(s)

1467-9

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Identifiers

DOI

10.1093/HMG/4.8.1467

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PubMed publication ID

7581392

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ResearchGate publication ID

15618525

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(Q28290728)

Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

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