(Q62936702)

English

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

article

In more languages

edit

Statements

instance of

scholarly article

0 references

title

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss (English)

0 references

1 reference

DA Scott

1

0 references

ML Kraft

series ordinal

2

0 references

R Carmi

series ordinal

3

0 references

A Ramesh

series ordinal

4

0 references

K Elbedour

series ordinal

5

0 references

Y Yairi

series ordinal

6

0 references

C. R. Srikumari Srisailapathy

series ordinal

7

0 references

SS Rosengren

series ordinal

8

0 references

AF Markham

series ordinal

9

0 references

RF Mueller

series ordinal

10

0 references

NJ Lench

series ordinal

11

0 references

G Van Camp

series ordinal

12

0 references

RJH Smith

series ordinal

13

0 references

VC Sheffield

series ordinal

14

0 references

publication date

1998

0 references

published in

Human Mutation

0 references

volume

11

0 references

issue

5

0 references

page(s)

387-394

0 references

Identifiers

DOI

10.1002/(SICI)1098-1004(1998)11:5<387::AID-HUMU6>3.0.CO;2-8

0 references

(Q62936702)

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)